Haplogroup I
Possible time of origin20.1 kya (Olivieri 2013)
Possible place of originWest Asia (Terreros 2011 and Fernandes 2012), or Southwest Asia
AncestorN1a1b (former N1e'I), (Olivieri 2013)
DescendantsI1, I2'3, I4, I5, I6, I7 (Olivieri 2013)
Defining mutationsT10034C, G16129A!, G16391A (Behar & Family Tree DNA 2012)

Haplogroup I is a human mitochondrial DNA (mtDNA) haplogroup. It is believed to have originated about 21,000 years ago, during the Last Glacial Maximum (LGM) period in West Asia ((Olivieri 2013); Terreros 2011; Fernandes 2012). The haplogroup is unusual in that it is now widely distributed geographically, but is common in only a few small areas of East Africa, West Asia and Europe. It is especially common among the El Molo and Rendille peoples of Kenya, various regions of Iran, the Lemko people of Slovakia, Poland and Ukraine, the island of Krk in Croatia, the department of Finistère in France and some parts of Scotland and Ireland.

Origin

Haplogroup I is a descendant (subclade) of haplogroup N1a1b and sibling of haplogroup N1a1b1 (Olivieri 2013). It is believed to have arisen somewhere in West Asia between 17,263 and 24,451 years before present (BP) (Behar 2012b), with coalescence age of 20.1 thousand years ago (Olivieri 2013). It has been suggested that its origin may be in Iran or more generally the Near East (Terreros 2011). It has diverged to at least seven distinct clades i.e. branches I1–I7, dated between 16–6.8 thousand years (Olivieri 2013). The hypothesis about its Near Eastern origin is based on the fact that all haplogroup I clades, especially those from Late Glacial period (I1, I4, I5, and I6), include mitogenomes from the Near East (Olivieri 2013). The age estimates and dispersal of some subclades (I1, I2’3, I5) are similar to those of major subclades of the mtDNA haplogroups J and T, indicating possible dispersal of the I haplogroup into Europe during the Late Glacial period (c. 18–12 kya) and postglacial period (c. 10–11 kya), several millennia before the European Neolithic period. Some subclades (I1a1, I2, I1c1, I3) show signs of the Neolithic diffusion of agriculture and pastoralism within Europe (Olivieri 2013).

It is noteworthy that, with the exception of its northern neighbor Azerbaijan, Iran is the only population in which haplogroup I exhibits polymorphic levels. Also, a contour plot based on the regional phylogeographic distribution of the I haplogroup exhibits frequency clines consistent with an Iranian cradle ... Moreover, when compared with other populations in the region, those from the Levant (Iraq, Syria and Palestine) and the Arabian Peninsula (Oman and UAE) exhibit significantly lower proportions of I individuals ... this haplogroup has been detected in European groups (Krk, a tiny island off the coast of Croatia (11.3%), and Lemko, an isolate from the Carpathian Highlands (11.3%)) at comparable frequencies to those observed in the North Iranian population. However, the higher frequencies of the haplogroup within Europe are found in geographical isolates and are likely the result of founder effects and/or drift ... it is plausible that the high levels of haplogroup I present in Iran may be the result of a localized enrichment through the action of genetic drift or may signal geographical proximity to the location of origin.

Terreros 2011

A similar view puts more emphasis on the Persian Gulf region of the Near East (Fernandes 2012).

Haplogroup I ... dates to ~25 ka ago and is overall most frequent in Europe ..., but the facts that it has a frequency peak in the Gulf region and that its highest diversity values are in the Gulf, Anatolia, and southeast Europe suggest that its origin is most likely in the Near East and/or Arabia ...

Distribution

Projected frequencies of mtDNA haplogroup I

Haplogroup I is found at moderate to low frequencies in East Africa, Europe, West Asia and South Asia (Fernandes 2012). In addition to the confirmed seven clades, the rare basal/paraphyletic clade I* has been observed in three individuals; two from Somalia and one from Iran (Olivieri 2013).

Africa

The highest frequencies of mitochondrial haplogroup I observed so far appear in the Cushitic-speaking El Molo (23%) and Rendille (>17%) in northern Kenya (Castrì 2008). The clade is also found at comparable frequencies among the Soqotri (~22%).[1]

Population Location Language Family N Frequency Source
AmharaEthiopiaAfro-Asiatic > Semitic1/1200.83%Kivisild 2004
EgyptiansEgyptAfro-Asiatic > Semitic2/345.9%Stevanovitch 2004
Beta IsraelEthiopiaAfro-Asiatic > Cushitic0/290.00%Behar 2008a
Dawro KontaEthiopiaAfro-Asiatic > Omotic0/1370.00%Castrì 2008 and Boattini 2013
EthiopiaEthiopiaUndetermined0/770.00%Soares 2011
Ethiopian JewsEthiopiaAfro-Asiatic > Cushitic0/410.00%Non 2011
GurageEthiopiaAfro-Asiatic > Semitic1/214.76%Kivisild 2004
HamerEthiopiaAfro-Asiatic > Omotic0/110.00%Castrì 2008 and Boattini 2013
OngotaEthiopiaAfro-Asiatic > Cushitic0/190.00%Castrì 2008 and Boattini 2013
OromoEthiopiaAfro-Asiatic > Cushitic0/330.00%Kivisild 2004
TigraiEthiopiaAfro-Asiatic > Semitic0/440.00%Kivisild 2004
DaasanachKenyaAfro-Asiatic > Cushitic0/490.00%Poloni 2009
ElmoloKenyaAfro-Asiatic > Cushitic12/5223.08%Castrì 2008 and Boattini 2013
LuoKenyaNilo-Saharan0/490.00%Castrì 2008 and Boattini 2013
MaasaiKenyaNilo-Saharan0/810.00%Castrì 2008 and Boattini 2013
NairobiKenyaNiger-Congo0/1000.00%Brandstatter 2004
NyangatomKenyaNilo-Saharan1/1120.89%Poloni 2009
RendilleKenyaAfro-Asiatic > Cushitic3/1717.65%Castrì 2008 and Boattini 2013
SamburuKenyaNilo-Saharan3/358.57%Castrì 2008 and Boattini 2013
TurkanaKenyaNilo-Saharan0/510.00%Castrì 2008 and Boattini 2013
HutuRwandaNiger-Congo0/420.00%Castrì 2009
DinkaSudanNilo-Saharan0/460.00%Krings 1999
SudanSudanUndetermined0/1020.00%Soares 2011
BurungeTanzaniaAfro-Asiatic > Cushitic1/382.63%Tishkoff 2007
DatogaTanzaniaNilo-Saharan0/570.00%Tishkoff 2007 and Knight 2003
IraqwTanzaniaAfro-Asiatic > Cushitic0/120.00%Knight 2003
SukumaTanzaniaNiger-Congo0/320.00%Tishkoff 2007 and Knight 2003
TuruTanzaniaNiger-Congo0/290.00%Tishkoff 2007
YemeniYemenAfro-Asiatic > Semitic0/1140.00%Kivisild 2004

Asia

Haplogroup I is present across West Asia and Central Asia, and is also found at trace frequencies in South Asia. Its highest frequency area is perhaps in northern Iran (9.7%). Terreros 2011 notes that it also has high diversity there and reiterates past studies that have suggested that this may be its place of origin. Found in Svan population from Georgia(Caucasus) I* 4.2%."Sequence polymorphisms of the mtDNA control region in a human isolate: the Georgians from Swanetia."Alfonso-Sánchez MA1, Martínez-Bouzas C, Castro A, Peña JA, Fernández-Fernández I, Herrera RJ, de Pancorbo MM. The table below shows some of the populations where it has been detected.

Population Language Family N Frequency Source
BaluchIndo-European0/390.00%Quintana-Murci 2004
BrahuiDravidian0/380.00%Quintana-Murci 2004
Caucasus (Georgia)*Kartvelian1/581.80%Quintana-Murci 2004
Druze11/3113.54%Shlush 2008
GilakiIndo-European0/370.00%Quintana-Murci 2004
GujaratiIndo-European0/340.00%Quintana-Murci 2004
HazaraIndo-European0/230.00%Quintana-Murci 2004
Hunza BurushoIsolate2/444.50%Quintana-Murci 2004
India8/25440.30%Metspalu 2004
Iran (North)3/319.70%Terreros 2011
Iran (South)2/1171.70%Terreros 2011
KalashIndo-European0/440.00%Quintana-Murci 2004
Kurdish (Western Iran)Indo-European1/205.00%Quintana-Murci 2004
Kurdish (Turkmenistan)Indo-European1/323.10%Quintana-Murci 2004
LurIndo-European0/170.00%Quintana-Murci 2004
MakraniIndo-European0/330.00%Quintana-Murci 2004
MazandarianIndo-European1/214.80%Quintana-Murci 2004
PakistaniIndo-European0/1000.00%Quintana-Murci 2004
Pakistan1/1450.69%Metspalu 2004
ParsiIndo-European0/440.00%Quintana-Murci 2004
PathanIndo-European1/442.30%Quintana-Murci 2004
PersianIndo-European1/422.40%Quintana-Murci 2004
ShugnanIndo-European1/442.30%Quintana-Murci 2004
SindhiIndo-European1/238.70%Quintana-Murci 2004
Turkish (Azerbaijan)Turkic2/405.00%Quintana-Murci 2004
Turkish (Anatolia)*Turkic1/502.00%Quintana-Murci 2004
TurkmenTurkic0/410.00%Quintana-Murci 2004
UzbekTurkic0/420.00%Quintana-Murci 2004

Europe

Eastern Europe

In Eastern Europe, the frequency of haplogroup I is generally lower than in Western Europe (1 to 3 percent), but its frequency is more consistent between populations with fewer places of extreme highs or lows. There are two notable exceptions. Nikitin 2009 found that Lemkos (a sub- or co-ethnic group of Rusyns) in the Carpathian mountains have the "highest frequency of haplogroup I (11.3%) in Europe, identical to that of the population of Krk Island (Croatia) in the Adriatic Sea".[Footnote 1][Footnote 2]

Population N Frequency Source
Boyko0/200.00%Nikitin 2009
Hutsul0/380.00%Nikitin 2009
Lemko6/5311.32%Nikitin 2009
Belorussians2/922.17%Belyaeva 2003
Russia (European)3/2151.40%Helgason 2001
Romanians (Constanta)590.00%Bosch 2006
Romanians (Ploiesti)462.17%Bosch 2006
Russia1/502.0%Malyarchuk 2001
Ukraine0/180.00%Malyarchuk 2001
Croatia (Mainland)4/2771.44%Pericić 2005
Croatia (Krk)15/13311.28%Cvjetan 2004
Croatia (Brač)1/1050.95%Cvjetan 2004
Croatia (Hvar)2/1081.9%Cvjetan 2004
Croatia (Korčula)1/981%Cvjetan 2004
Herzegovinians1/1300.8%Cvjetan 2004
Bosnians6/2472.4%Cvjetan 2004
Serbians4/1173.4%Cvjetan 2004
Macedonians2/1461.4%Cvjetan 2004
Macedonian Romani7/1534.6%Cvjetan 2004
Slovenians2/1041.92%Malyarchuk 2003
Bosnians4/1442.78%Malyarchuk 2003
Poles8/4361.83%Malyarchuk 2003
Caucasus (Georgia)*1/581.80%Quintana-Murci 2004
Russians5/2012.49%Malyarchuk 2003
Bulgaria/Turkey2/1021.96%Helgason 2001


Western Europe

In Western Europe, haplogroup I is most common in Northwestern Europe (Norway, the Isle of Skye, and the British Isles). The frequency in these areas is between 2 and 5 percent. Its highest frequency in Brittany, France where it is over 9 percent of the population in Finistère. It is uncommon and sometimes absent in other parts of Western Europe (Iberia, South-West France, and parts of Italy).

Population Language N Frequency Source
Austria/Switzerland4/1872.14%Helgason 2001
Basque (Admix Zone)Basque/Labourdin côtier-haut navarrais0/560.00%Martınez-Cruz 2012
Basque (Araba)Basque/Occidental0/550.00%Martınez-Cruz 2012
Basque (Bizkaia)Basque/Biscayen1/591.69%Martınez-Cruz 2012
Basque (Central/Western Navarre )Basque/Haut-navarrais méridional2/633.17%Martınez-Cruz 2012
Basque (Gipuskoa)Basque/Gipuzkoan0/570.00%Martınez-Cruz 2012
Basque (Navarre Labourdin)Basque/Bas-navarrais0/680.00%Martınez-Cruz 2012
Basque (North/Western Navarre)Basque/Haut-navarrais septentrional0/510.00%Martınez-Cruz 2012
Basque (Roncal)Basque/Roncalais-salazarais0/550.00%Martınez-Cruz 2012
Basque (Soule)Basque/Souletin0/620.00%Martınez-Cruz 2012
Basque (South/Western Gipuskoa)Basque/Biscayen0/640.00%Martınez-Cruz 2012
BéarnFrench0/510.00%Martınez-Cruz 2012
BigorreFrench0/440.00%Martınez-Cruz 2012
BurgosSpanish0/250.00%Martınez-Cruz 2012
CantabriaSpanish0/180.00%Martınez-Cruz 2012
ChalosseFrench0/580.00%Martınez-Cruz 2012
Denmark6/1055.71%Mikkelsen 2010
England/Wales12/4293.03%Helgason 2001
Finland1/492.04%Torroni 1996
Finland/Estonia5/2022.48%Helgason 2001
France (Finistère)2/229.10%Dubut 2003
France (Morbihan)0/400.00%Dubut 2003
France (Normandy)0/390.00%Dubut 2003
France (Périgord-Limousin)-2/722.80%Dubut 2003
France (Var)2/375.40%Dubut 2003
France/Italy2/2480.81%Helgason 2001
Germany12/5272.28%Helgason 2001
Iceland21/4674.71%Helgason 2001
Ireland3/1282.34%Helgason 2001
Italy (Tuscany)2/484.20%Torroni 1996
La RiojaSpanish1/511.96%Martınez-Cruz 2012
North AragonSpanish0/260.00%Martınez-Cruz 2012
Orkney5/1523.29%Helgason 2001
Saami0/1760.00%Helgason 2001
Scandinavia12/6451.86%Helgason 2001
Scotland39/8914.38%Helgason 2001
Spain/Portugal2/3520.57%Helgason 2001
Sweden0/370.00%Torroni 1996
Western BizkaiaSpanish0/180.00%Martınez-Cruz 2012
Western Isles/Isle of Skye15/2466.50%Helgason 2001

Historic and prehistoric samples

Haplogroup I has until recently been absent from ancient European samples found in Paleolithic and Mesolithic grave sites. In 2017, in a site on Italian island of Sardinia was found a sample with the subclade I3 dated to 9124–7851 BC (Modi 2017), while in the Near East, in Levant was found a sample with yet-not-defined subclade dated 8850–8750 BC, while in Iran was found a younger sample with subclade I1c dated to 3972–3800 BC (Lazaridis 2016). In Neolithic Spain (c. 6090–5960 BC in Paternanbidea, Navarre) was found a sample with yet-not-defined subclade (Olivieri 2013). Haplogroup I displays a strong connection with the Indo-European migrations; especially its I1, I1a1 and I3a subclades, which have been found in Poltavka and Srubnaya cultures in Russia (Mathieson 2015), among ancient Scythians (Der Sarkissian 2011), and in Corded Ware and Unetice Culture burials in Saxony (Brandt 2013).I3a has also been found in the Unetice Culture in Lubingine, Germany 2,200 B.C. to 1,800 B.C. courtesy article on Unetice Culture Wikipedia of 2 Skeletons that were DNA tested. Haplogroup I (with undetermined subclades) has also been noted at significant frequencies in more recent historic grave sites (Melchior 2008 and Hofreiter 2010).

In 2013, Nature announced the publication of the first genetic study utilizing next-generation sequencing to ascertain the ancestral lineage of an Ancient Egyptian individual. The research was led by Carsten Pusch of the University of Tübingen in Germany and Rabab Khairat, who released their findings in the Journal of Applied Genetics. DNA was extracted from the heads of five Egyptian mummies that were housed at the institution. All the specimens were dated to between 806 BC and 124 AD, a time frame corresponding with the Late Dynastic and Ptolemaic periods. The researchers observed that one of the mummified individuals likely belonged to the I2 subclade.[2] Haplogroup I has also been found among ancient Egyptian mummies excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which date from the Pre-Ptolemaic/late New Kingdom, Ptolemaic, and Roman periods.[3]

Haplogroup I5 has also been observed among specimens at the mainland cemetery in Kulubnarti, Sudan, which date from the Early Christian period (AD 550–800).[4]

Samples with determined subclades

Culture Country Site Date Haplogroup Source
UneticeGermanyEsperstedt2050–1800 BCI1Adler 2012; Brandt 2013
Bell BeakerGermany2600–2500 BCI1a1Lee 2012; Oliveiri 2013
UneticeGermanyPlotzkau 32200–1550 BCI1a1Brandt 2013
UneticeGermanyEulau1979–1921 BCI1a1Brandt 2013
SrubnayaRussiaRozhdestveno I, Samara Steppes, Samara1850–1600 BCI1a1Mathieson 2015
Seh GabiIran3972–3800 BCI1cLazaridis 2016
Cami de Can GrauSpain3500–3000 BCI1c1Sampietro 2007; Olivieri 2013
Late Dynastic-PtolemaicEgypt806 BC – 124 ADI2Khairat 2013
Su CarroppuItaly9124–7851 BCI3Modi 2017
ScythianRussiaRostov-on-Don500–200 BCI3Der Sarkissian 2011
UneticeGermanyBenzingerode-Heimburg1653–1627 BCI3aBrandt 2013
UneticeGermanyEsperstedt2131–1979 BCI3aAdler 2012; Brandt 2013; Haak 2015; Mathieson 2015
UneticeGermanyEsperstedt2199–2064 BCI3aAdler 2012; Brandt 2013; Haak 2015
PoltavkaRussiaLopatino II, Sok River, Samara2885–2665 BCI3aMathieson 2015
KarasukRussiaSabinka 21416–1268 BCI4a1Allentoft 2015
MinoanGreeceAyios Charalambos2400–1700 BCI5Hughey 2013
MinoanGreeceAyios Charalambos2400–1700 BCI5Hughey 2013
MinoanGreeceAyios Charalambos2400–1700 BCI5Hughey 2013
Christian NubiaSudanKulubnarti550–800 ADI5Sirak 2016
Late Bronze AgeArmeniaNorabak1209–1009 BCI5cAllentoft 2015
MezhovskavaRussiaKapova cave1598–1398 BCI5cAllentoft 2015

Samples with unknown subclades

Populations N Frequency Source
Roman Iron Age sites
Bøgebjerggård (AD 1–400)
Simonsborg (AD 1–200)
Skovgaarde (AD 200–400)
3/24 12.5% Melchior 2008a, Hofreiter 2010
Viking Age burial sites
Galgedil (AD 1000)
Christian cemetery Kongemarken (AD 1000–1250)
medieval cemetery Riisby (AD 1250–1450)
4/29 13.79% Melchior 2008, Hofreiter 2010
Anglo-Saxon burial sites
Leicester:6
Lavington:6
Buckland:7
Norton:12
Norwich:17
1/48 2.08% Töpf 2006

We have previously observed a high frequency of Hg I's among Iron Age villagers (Bøgebjerggård) and individuals from the early Christian cemetery, Kongemarken [16], [17]. This trend was also found for the additional sites reported here, Simonsborg, Galgedil and Riisby. The overall frequency of Hg I among the individuals from the Iron Age to the Medieval Age is 13% (7/53) compared to 2.5% for modern Danes [35]. The higher frequencies of Hg I can not be ascribed to maternal kinship since only two individuals share the same common motif (K2 and K7 at Kongemarken). Except for Skovgaarde (no Hg I's observed) frequencies range between 9% and 29% and there seems to be no trend in relation to time. No Hg I's were observed at the Neolithic Damsbo and the Bronze Age site Bredtoftegård, where all three individuals harbored Hg U4 or Hg U5a (Table 1).

Hofreiter 2010

The frequency of haplogroup I may have undergone a reduction in Europe following the Middle Ages. An overall frequency of 13% was found in ancient Danish samples from the Iron Age to the Medieval Age (including Vikings) from Denmark and Scandinavia compared to only 2.5% in modern samples. As haplogroup I is not observed in any ancient Italian, Spanish [contradicted by the recent research as have been found in pre-Neolithic Italy as well Neolithic Spain], British, central European populations, early central European farmers and Neolithic samples, according to the authors "Haplogroup I could, therefore, have been an ancient Southern Scandinavian type "diluted" by later immigration events" (Hofreiter 2010).

Subclades

Phylogenetic tree of haplogroups I (left) and W (right). Kya in the left scale bar stands for thousand years ago (Olivieri 2013).

Tree

This phylogenetic tree of haplogroup I subclades with time estimates is based on the paper and published research (Olivieri 2013).

Hg (July 2013) Age estimate (thousand years) 95% confidence interval (thousand years)
N1a1b28.623.5–33.9
I20.118.4–21.9
I116.314.6–18.0
I1a11.69.9–13.3
I1a14.94.2–5.6
I1a1a3.83.3–4.4
I1a1b1.40.5–2.2
I1a1c2.51.3–3.7
I1a1d1.81.0–2.6
I1b13.411.3–15.5
I1c10.38.4–12.2
I1c17.25.4–9.0
I1c1a4.02.5–5.4
I2'312.610.4–14.7
I26.86.0–7.6
I2a4.73.8–5.7
I2a13.22.1–4.4
I2b1.70.5–2.9
I2c4.73.6–5.8
I2d3.01.1–4.8
I2e3.11.4–4.8
I310.68.8–12.4
I3a7.46.1–8.7
I3a16.14.7–7.5
I3b2.61.1–4.2
I3c9.47.6–11.2
I415.112.3–18.0
I4a6.45.4–7.4
I4a15.74.5–6.7
I4b8.45.8–10.9
I518.416.4–20.3
I5a16.014.0–17.9
I5a19.27.1–11.3
I5a212.310.2–14.4
I5a2a1.61.0–2.1
I5a34.82.8–6.8
I5a45.63.5–7.8
I5b8.86.3–11.2
I618.416.2–20.6
I6a5.33.5–7.0
I6b13.110.4–15.8
I79.16.3–11.9

Distribution

I1

Haplogroup I1
Possible time of origin15,231 ± 3,402 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutations455.1T, G6734A, G9966A, T16311C! (Behar & Family Tree DNA 2012)

It formed during the Last Glacial pre-warming period. It is found mainly in Europe, Near East, occasionally in North Africa and the Caucasus. It is the most frequent clade of the haplogroup (Olivieri 2013).

Genbank IDPopulationSource
JQ702472Behar 2012b
JQ702567GermanyBehar 2012b
JQ704077GermanyBehar 2012b
JQ705190Behar 2012b
JQ705840Behar 2012b
KY022422IranFamilyTreeDNA
MG191350SpanishFamilyTreeDNA
MG646219PolandPiotrowska-Nowak 2019b
MK294405SwedishFamilyTreeDNA
MN586593GermanyFamilyTreeDNA
MW600776RussianFamilyTreeDNA
I1a
Haplogroup I1a
Possible time of origin11,726 ± 3,306 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsT152C!, G207A (Behar & Family Tree DNA 2012)

The subclade frequency peaks (circa 2.8%) are mostly located in North-Eastern Europe (Olivieri 2013).

Genbank IDPopulationSource
EU694173FamilyTreeDNA
HM454265Turkey (Armenian)FamilyTreeDNA
JQ245746ChuvashFernandes 2012
KC911435IranDerenko 2013
KC911577IranDerenko 2013
MK217219AssyriansShamoon-Pour 2019
OQ982011ItalyFamilyTreeDNA
I1a1
Haplogroup I1a1
Possible time of origin5,294 ± 2,134 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a
Defining mutationsG203A, C3990T, G9947A, A9966G!, T10915C! (Behar & Family Tree DNA 2012)
Genbank IDPopulationSource
EF177414PortugalPereira 2007
FJ460562TunisiaCosta 2009
JQ245748CzechFernandes 2012
JQ245749CzechFernandes 2012
JQ245767TurkeyFernandes 2012
JQ245802MoroccoFernandes 2012
JQ702519Behar 2012b
JQ702882Behar 2012b
JQ703835Behar 2012b
JQ705025Behar 2012b
JQ705645Behar 2012b
JQ705889Behar 2012b
JX152861DenmarkRaule 2014
JX153351DenmarkRaule 2014
JX297189SpainCardoso 2013
KJ570782CzechFamilyTreeDNA
MG551928EnglandFamilyTreeDNA
MH120632PolandPiotrowska-Nowak 2019a
MK874614ScotlandFamilyTreeDNA
MK967511IrelandFamilyTreeDNA
OM194303KazakhsAskapuli 2022
OM238070ScottishFamilyTreeDNA
OP681985Canary IslandersGarcía-Olivares 2023
OP682630Canary IslandersGarcía-Olivares 2023
OP682053Canary IslandersGarcía-Olivares 2023
OP682263Canary IslandersGarcía-Olivares 2023
I1a1a
Haplogroup I1a1a
Possible time of origin3,327 ± 2,720 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsG9053A (Behar & Family Tree DNA 2012)
Genbank IDPopulationSource
AY339502FinlandFinnila 2001
AY339503FinlandFinnila 2001
AY339504FinlandFinnila 2001
AY339505FinlandFinnila 2001
JQ702939Behar 2012b
JQ703652Behar 2012b
JQ704013Behar 2012b
JQ705140Behar 2012b
JQ705378Behar 2012b
JX153234FinlandRaule 2014
KC170986UkrainianFamilyTreeDNA
KF146236PolandOlivieri 2013
KF146237ItalyOlivieri 2013
KY409854SardiniansOlivieri 2017
KY410140SardiniansOlivieri 2017
KY671032RussiaMalyarchuk 2017
KY671065RussiaMalyarchuk 2017
KY671085RussiaMalyarchuk 2017
MG646256PolandPiotrowska-Nowak 2019b
MG646266PolandPiotrowska-Nowak 2019b
MG952793HungaryMalyarchuk 2018
MH120465PolandPiotrowska-Nowak 2019a
MH120665PolandPiotrowska-Nowak 2019a
MK103008SwedishFamilyTreeDNA
MK202791RussianFamilyTreeDNA
MK732936FinnishFamilyTreeDNA
OL638786BrazilAvila 2022
OL638813BrazilAvila 2022
OM714626SlovakGrzybowski 2023
OM714682SlovakGrzybowski 2023
OM714689SlovakGrzybowski 2023
OM714735CzechGrzybowski 2023
OM714742CzechGrzybowski 2023
OR438500PolandPiotrowska-Nowak 2023
OR438613PolandPiotrowska-Nowak 2023
I1a1a1
GenBank IDPopulationSource
AY339506FinlandFinnila 2001
KF899911RussiaFamilyTreeDNA
JX152986FinlandRaule 2014
MH983007FinlandFamilyTreeDNA
MK040467FinlandFamilyTreeDNA
I1a1a2
GenBank IDPopulationSource
AY339507FinlandFinnila 2001
AY339508FinlandFinnila 2001
AY339509FinlandFinnila 2001
OL555719FinnishYSEQ
I1a1b
Haplogroup I1a1b
Possible time of origin2,608 ± 2,973 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsT14182C (Behar & Family Tree DNA 2012)
Genbank IDPopulationSource
JQ702470Behar 2012b
JQ704690Behar 2012b
JQ705595Behar 2012b
JX153797DenmarkRaule 2014
JX154050DenmarkRaule 2014
KF586486IrelandFamilyTreeDNA
KJ849732SwedesFamilyTreeDNA
KJ850479EnglishFamilyTreeDNA
KM822854ScotlandFamilyTreeDNA
KT074442FinlandFamilyTreeDNA
KU672519IrelandFamilyTreeDNA
KX906927IrelandFamilyTreeDNA
MG182421IrelandFamilyTreeDNA
MG548632WelshFamilyTreeDNA
MN163828FinlandFamilyTreeDNA
MT984338IrelandYSEQ
MZ457933IrelandFamilyTreeDNA
MZ846395ShetlandDulias 2022
I1a1c
Haplogroup I1a1c
Possible time of originAbout 1,523 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsT6620C (Behar & Family Tree DNA 2012)
Genbank IDPopulationSource
GU123027Mishar Tatars
(Buinsk)
Malyarchuk 2010b
JQ702023Behar 2012b
JQ702457Behar 2012b
KF146238UkraineOlivieri 2013
MG386697GermanFamilyTreeDNA
MH918097LithuaniaFamilyTreeDNA
OL638548BrazilAvila 2022
OM714767CzechGrzybowski 2023
I1a1d
Haplogroup I1a1d
Possible time of originAbout 1,892 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsA1836G, T4023C, T13488C, T16189C! (Behar & Family Tree DNA 2012)
Genbank IDPopulationSource
JQ702342Behar 2012b
JQ705189Behar 2012b
KT124612WalesFamilyTreeDNA
KX949567United KingdomFamilyTreeDNA
MZ846966OrkneyDulias 2022
OQ101207EnglishFamilyTreeDNA
OR193751WalesFamilyTreeDNA
I1a1e
GenBank IDPopulationSource
JQ701900Behar 2012b
JQ702820Behar 2012b
KJ095105IrelandFamilyTreeDNA
KU375199EnglandFamilyTreeDNA
KY671114RussiaMalyarchuk 2017
MK570297EnglandFamilyTreeDNA
MN599048NorwayFamilyTreeDNA
MZ846316ShetlandDulias 2022
MZ846989OrkneyDulias 2022
MZ847013OrkneyDulias 2022
MZ847773OrkneyDulias 2022
MZ847969OrkneyDulias 2022
MZ848045OrkneyDulias 2022
I1b
Haplogroup I1b
Possible time of origin11,135 ± 4,818 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsT6227C (Behar & Family Tree DNA 2012)
Genbank IDPopulationSource
AY195769CaucasianMishmar 2003
AY714041IndiaPalanichamy 2004
EF556153Jewish DiasporaBehar 2008a
FJ234984ArmenianFamilyTreeDNA
FJ968796FamilyTreeDNA
JQ704018Behar 2012b
JQ705376Behar 2012b
KC911562IranDerenko 2013
KF146240ItalyOlivieri 2013
KF146241IranOlivieri 2013
KF146242IranOlivieri 2013
KF146243ItalyOlivieri 2013
KJ890387.1SwedishFamilyTreeDNA
KJ890390GermanFamilyTreeDNA
KJ937089ArmenianFamilyTreeDNA
KM986573YemenVyas 2016
KM986617YemenVyas 2016
KY073882HungaryFamilyTreeDNA
KY410160SardiniansOlivieri 2017
KY671121RussiaMalyarchuk 2017
KY680312SwedenFamilyTreeDNA
MF362869ArmenianMargaryan 2017
MG272907ThailandKutanan 2018
MH378689ChechenFamilyTreeDNA
MK491399ArmenianDerenko 2019
MN595812PakistanRahman 2021
MW959772EnglishFamilyTreeDNA
OM714633SlovakGrzybowski 2023
OR838478Saudi ArabiaFamilyTreeDNA
I1c
Haplogroup I1c
Possible time of origin8,216 ± 3,787 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsG8573A, C16264T, G16319A, T16362C (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
JQ705932Behar 2012b
KP783168TurkishFamilyTreeDNA
MG748728SpainFamilyTreeDNA
OL619849MongoliaCardinali 2022
OR769030TurkeyYSEQ
I1c1
GenBank IDPopulationSource
KF146244ItalyOlivieri 2013
MF437134United Arab EmiratesAl-Jasmi 2020
MH120606PolandPiotrowska-Nowak 2019a
OL638549BrazilAvila 2022
I1c1a1
GenBank IDPopulationSource
EU564849FamilyTreeDNA
JQ702655Behar 2012b
JQ705364Behar 2012b
KJ558222LithuaniaFamilyTreeDNA
KJ801472-Lang 2015
KU052787LithuaniaFamilyTreeDNA
MZ158184BelarusFamilyTreeDNA
OR182493Hungarian JewsBrook 2022
I1c1a2
GenBank IDPopulationSource
KX156834ChechensFamilyTreeDNA
I1d
GenBank IDPopulationSource
KF146245ItalyOlivieri 2013
KF146246ItalyOlivieri 2013
I1e
GenBank IDPopulationSource
JX462710IndiaKhan 2013
KY697192ItaliansFamilyTreeDNA
KY982964-FamilyTreeDNA
I1f
GenBank IDPopulationSource
JX153931DenmarkRaule 2014
JX153979DenmarkRaule 2014
KF251094EnglishFamilyTreeDNA
KJ557251ScottishFamilyTreeDNA
KJ809106EnglandFamilyTreeDNA
MK434282NorwayFamilyTreeDNA

I2'3

Haplogroup I2'3
Possible time of origin11,308 ± 4,154 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsT152C!, G207A (Behar & Family Tree DNA 2012)

It is the common root clade for subclades I2 and I3. There's a sample from Tanzania with which I2'3 shares a variant at position 152 from the root node of haplogroup I, and this "node 152" could be upstream I2'3s clade (Olivieri 2013). Both I2 and I3 might have formed during the Holocene period, and most of their subclades are from Europe, only few from the Near East (Olivieri 2013). Examples of this ancestral branch have not been documented.

I2
Haplogroup I2
Possible time of origin6,387 ± 2,449 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2'3
Defining mutationsA15758G (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
EU570217IrelandFamilyTreeDNA
FJ911909FamilyTreeDNA
GU122984Volga TatarsMalyarchuk 2010b
GU294854FamilyTreeDNA
HQ287882Pope 2011
JQ701942Behar 2012b
JQ702191Behar 2012b
JQ702284Behar 2012b
JQ703850Behar 2012b
JQ704705Behar 2012b
JQ704765Behar 2012b
JQ704936Behar 2012b
JQ705000Behar 2012b
JQ705304Behar 2012b
JQ705379Behar 2012b
JQ245744ChechnyaFernandes 2012
JQ245747CzechFernandes 2012
JQ245771TurkeyFernandes 2012
JX153641DenmarkRaule 2014
JX153773DenmarkRaule 2014
KC911614Iranian AzerbaijanisDerenko 2013
KF146254ItalyOlivieri 2013
KF146255UkraineOlivieri 2013
KF146256ItalyOlivieri 2013
KF146257ItalyOlivieri 2013
KJ599625ChechensFamilyTreeDNA
KJ645815ArmeniansFamilyTreeDNA
KP969064NorwayFamilyTreeDNA
KR014102ItalyFamilyTreeDNA
KU682980UyghursZheng 2018
KU683033UyghursZheng 2018
KU683240UyghursZheng 2018
KU683502UyghursZheng 2018
KY000078NorwayFamilyTreeDNA
KY042020SwedenFamilyTreeDNA
KY172919SwedenFamilyTreeDNA
KY428665EnglandFamilyTreeDNA
KY671062RussiaMalyarchuk 2017
KY671122RussiaMalyarchuk 2017
KY780115IrishFamilyTreeDNA
MF068709GermanyFamilyTreeDNA
MF116368SwedenFamilyTreeDNA
MF279144SwedenFamilyTreeDNA
MF278022EnglandFamilyTreeDNA
MF362766ArmeniansMargaryan 2017
MN540393EnglandFamilyTreeDNA
MT075870IrelandFamilyTreeDNA
MT223153IrelandFamilyTreeDNA
MZ846734ShetlandDulias 2022
MZ847795OrkneyDulias 2022
OM936970NetherlandsFamilyTreeDNA
ON060656IrelandFamilyTreeDNA
I2a
Haplogroup I2a
Possible time of origin3,771 ± 2,143 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsA11065G, G16145A (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
HQ326985FamilyTreeDNA
HQ714959ScotlandFamilyTreeDNA
JQ705921Behar 2012b
HQ695930FamilyTreeDNA
I2a1
Haplogroup I2a1
Possible time of origin2,986 ± 1,968 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2a
Defining mutationsT3398C (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
AY339497FinlandFinnila 2001
HQ724528IrelandFamilyTreeDNA
JN411083IrelandFamilyTreeDNA
I2a1a
GenBank IDPopulationSource
MT892955FinlandFamilyTreeDNA
I2a2
GenBank IDPopulationSource
JQ703910Behar 2012b
KP987219IrelandFamilyTreeDNA
KR088263EnglandFamilyTreeDNA
I2a3
GenBank IDPopulationSource
JQ705175Behar 2012b
JX154048DenmarkRaule 2014
KU493988SwedenFamilyTreeDNA
MK591009IrelandFamilyTreeDNA
MT137386IrelandFamilyTreeDNA
I2b
Haplogroup I2b
Possible time of originAbout 1,267 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsT6515C, 8281-8289d, A16166c (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
AY339498FinlandFinnila 2001
AY339499FinlandFinnila 2001
AY339500FinlandFinnila 2001
AY339501FinlandFinnila 2001
I2c
Haplogroup I2c
Possible time of originAbout 2,268 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsT460C, G9438A (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
JQ702163Behar 2012b
JQ702253Behar 2012b
JQ703024Behar 2012b
JQ705187Behar 2012b
JQ705666Behar 2012b
KJ882427FranceFamilyTreeDNA
KR051235ScotlandFamilyTreeDNA
KU291444ScotlandFamilyTreeDNA
MZ846506ShetlandDulias 2022
MZ846570ShetlandDulias 2022
MZ847001OrkneyDulias 2022
MZ847048OrkneyDulias 2022
OL604518ScotlandFamilyTreeDNA
OP682030Canary IslandersGarcía-Olivares 2023
I2d
Haplogroup I2d
Possible time of originAbout 3,828 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsG6480A (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
JQ705244Behar 2012b
JQ703829Behar 2012b
JX153642DenmarkRaule 2014
KY684194GermansFamilyTreeDNA
MG646226PolandPiotrowska-Nowak 2019b
MH087474EnglishFamilyTreeDNA
MH120469PolandPiotrowska-Nowak 2019a
MH120515PolandPiotrowska-Nowak 2019a
MH675881FinlandFamilyTreeDNA
I2e
Haplogroup I2e
Possible time of originAbout 2,936 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsG3591A (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
JQ702578Behar 2012b
JQ703106Behar 2012b
MN176248PolandPiotrowska-Nowak 2020
MN176270PolandPiotrowska-Nowak 2020
I3
Haplogroup I3
Possible time of origin8,679 ± 3,410 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2'3
Defining mutationsT239C (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
JQ702647Behar 2012b
JQ703862Behar 2012b
OL521838IrelandFamilyTreeDNA
I3a
Haplogroup I3a
Possible time of origin6,091 ± 3,262 BP (Behar 2012b)
Possible place of originOldest sample from Poltavka culture (Russia-Lopatino II, Sok River, Samara, 2885–2665 BC) (Mathieson 2015)
AncestorI3
Defining mutationsT16086C (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
EU746658FranceFamilyTreeDNA
EU869314FamilyTreeDNA
JQ245751GreeceFernandes 2012
JQ702041Behar 2012b
JQ702062Behar 2012b
JQ702109Behar 2012b
JQ702413Behar 2012b
JX153712DenmarkRaule 2014
KF146258IranOlivieri 2013
KJ507246FlemishFamilyTreeDNA
KJ850495EnglishFamilyTreeDNA
KU859398BelgiumFamilyTreeDNA
KY369150ItalyFamilyTreeDNA
KY408233SardiniansOlivieri 2017
MF002495GermanyFamilyTreeDNA
MF322516IrishFamilyTreeDNA
MK088054FranceFamilyTreeDNA
MZ614451ScotlandFamilyTreeDNA
ON980565ScotlandFamilyTreeDNA
OP682222Canary IslandersGarcía-Olivares 2023
OP682259Canary IslandersGarcía-Olivares 2023
OP682273Canary IslandersGarcía-Olivares 2023
OP682309Canary IslandersGarcía-Olivares 2023
OP682392Canary IslandersGarcía-Olivares 2023
OP682401Canary IslandersGarcía-Olivares 2023
OQ470330NorwegiansFamilyTreeDNA
I3a1
Haplogroup I3a1
Possible time of origin5,070 ± 3,017 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI3a
Defining mutationsG2849A (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
AY963586ItalyBandelt
HQ420832FranceFamilyTreeDNA
JQ704837Behar 2012b
KP903567AustriaFamilyTreeDNA
MH120756PolandPiotrowska-Nowak 2019a
OL638572BrazilAvila 2022
I3b
Haplogroup I3b
Possible time of origin5,596 ± 3,629 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI3
Defining mutationsC16494T (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
GU590993IrelandFamilyTreeDNA
JQ705377Behar 2012b
I3c
GenBank IDPopulationSource
JQ702493Behar 2012b
JQ703883Behar 2012b
KJ021060-FamilyTreeDNA
I3d
GenBank IDPopulationSource
OR233329RussiansFamilyTreeDNA
OR438549PolandPiotrowska-Nowak 2023

I4

Haplogroup I4
Possible time of origin14,913 ± 5,955 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsG8519A (Behar & Family Tree DNA 2012)

The clade splits into subclades I4a and newly defined I4b, with samples found in Europe, the Near East and the Caucasus (Olivieri 2013).

GenBank IDPopulationSource
KJ021059FamilyTreeDNA
I4a
Haplogroup I4a
Possible time of originAbout 2,124 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI4
Defining mutationsA10819G (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
EU091245FamilyTreeDNA
JN660158ArmenianFamilyTreeDNA
JQ701909Behar 2012b
JQ701957Behar 2012b
JQ705303Behar 2012b
JQ705514Behar 2012b
JQ706017Behar 2012b
JQ702369Behar 2012b
JX153325DenmarkRaule 2014
KJ676862French CanadiansFamilyTreeDNA
KT390700IrelandFamilyTreeDNA
KX495667ArmenianFamilyTreeDNA
MF362868ArmeniansMargaryan 2017
MG660526ChelkansNazhmidenova 2020
MZ846849OrkneyDulias 2022
MZ846865OrkneyDulias 2022
OL638882BrazilAvila 2022
ON457162FamilyTreeDNA
ON602072EnglandFamilyTreeDNA
OQ645346GermanFamilyTreeDNA
I4a1
GenBank IDPopulationSource
EF153786SiberiaDerenko 2007
EF660987ItalyGasparre 2007
HM804481FamilyTreeDNA
JQ705060Behar 2012b
JQ705191Behar 2012b
JQ705906Behar 2012b
KJ676824GermanFamilyTreeDNA
KJ890389RussiaFamilyTreeDNA
KU922938WalesFamilyTreeDNA
KY849396SwedesFamilyTreeDNA
MG015877SwedesFamilyTreeDNA
MG646165PolandPiotrowska-Nowak 2019b
MH322053GermanyFamilyTreeDNA
MW691107IrelandFamilyTreeDNA
ON010030SwedenFamilyTreeDNA
I4a2
GenBank IDPopulationSource
KF254840FinlandFamilyTreeDNA
I4b
GenBank IDPopulationSource
JQ704976Behar 2012b
KF146261IranOlivieri 2013
KX467275IndiaSharma 2018
MG744604GermanyFamilyTreeDNA

I5

Haplogroup I5
Possible time of origin18,806 ± 4,005 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsA14233G (Behar & Family Tree DNA 2012)

Is the second most frequent clade of the haplogroup. Its subclades are found in Europe, e.g. I5a1, and the Near East, e.g. I5a2a and I5b (Olivieri 2013).

GenBank IDPopulationSource
HQ658465German (north)FamilyTreeDNA
JQ245724North OssetiaFernandes 2012
KJ920750German (west)FamilyTreeDNA
KT250729German (east)FamilyTreeDNA
KT346427PolishFamilyTreeDNA
MK617274SerbiaDavidovic 2020
I5a
Haplogroup I5a
Possible time of origin15,116 ± 4,128 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI5
Defining mutationsT5074C, C16148T (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
KT748522Pontic GreeksFamilyTreeDNA
KX017466FinnishFamilyTreeDNA
MF362944ArmeniansMargaryan 2017
MN696689FinnishFamilyTreeDNA
I5a1
Haplogroup I5a1
Possible time of origin11,062 ± 4,661 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI5a
Defining mutations8281-8289d, A12961G (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
JQ245807BulgariaFernandes 2012
JX152976FinlandRaule 2014
KM925143FinlandFamilyTreeDNA
MK134361SerbiaDavidovic 2020
MK217239AssyriansShamoon-Pour 2019
MT338490GermanyFamilyTreeDNA
I5a1a
GenBank IDPopulationSource
JQ705096Behar 2012b
KF146248ItalyOlivieri 2013
KJ746501EnglishFamilyTreeDNA
KX856070EnglishFamilyTreeDNA
MG744602FrenchFamilyTreeDNA
I5a1b
GenBank IDPopulationSource
AF382007LeonMaca-Meyer 2001
EF660917ItalyGasparre 2007
JQ704713Behar 2012b
I5a1c
GenBank IDPopulationSource
EU597573Bedouin (Israel)Hartmann 2009
JQ704768Behar 2012b
KF146247ItalyOlivieri 2013
I5a2
GenBank IDPopulationSource
JQ701894Behar 2012b
KY408295SardiniansOlivieri 2017
KY408387SardiniansOlivieri 2017
MH168104UkrainiansFamilyTreeDNA
MZ384391United KingdomFamilyTreeDNA
I5a2a
GenBank IDPopulationSource
JQ245733DubaiFernandes 2012
JQ245780YemenFernandes 2012
JQ245781YemenFernandes 2012
JQ245782YemenFernandes 2012
JQ245783YemenFernandes 2012
JQ245784YemenFernandes 2012
JQ245785YemenFernandes 2012
JQ245786YemenFernandes 2012
I5a3
GenBank IDPopulationSource
JN415483GermanyAchilli 2012
JQ245772TurkeyFernandes 2012
I5a4
GenBank IDPopulationSource
FJ348190HutteritePichler 2010
HM852869TurkeySchoenberg 2011
KF146249ItalyOlivieri 2013
KJ676977RomanianFamilyTreeDNA
KY615004RusynsFamilyTreeDNA
I5b
GenBank IDPopulationSource
KF255549ItalyFamilyTreeDNA
ON640629CyprusFamilyTreeDNA
I5c
GenBank IDPopulationSource
KM245143SpainFregel 2015
KP419690ItaliansFamilyTreeDNA
MF362879ArmeniansMargaryan 2017
MK491434ArmeniansDerenko 2019
OP642525ChechensFamilyTreeDNA
I5c1
GenBank IDPopulationSource
HQ658465GermansFamilyTreeDNA
KC787372EnglishFamilyTreeDNA
KF146251ItalyOlivieri 2013
KY409830SardiniansOlivieri 2017
KY981527SardiniansFamilyTreeDNA
OL438769RomaniansFamilyTreeDNA

I6

Haplogroup I6
Possible time of originAbout 18,400 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI
Defining mutationsT3645C (Behar & Family Tree DNA 2012)

The subclade is very rare, found until July 2013 only in four samples from the Near East (Olivieri 2013).

GenBank IDPopulationSource
JQ245773TurkeyFernandes 2012
MK036912CroatiaFamilyTreeDNA
I6a
Haplogroup I6a
Possible time of originAbout 5,300 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI6
Defining mutations(G203A), G3915A, A6116G, A7804G, T15287C, (A16293c) (Behar & Family Tree DNA 2012)
GenBank IDPopulationSource
AY245555Janssen 2006
JQ705382Behar 2012b
KM262180ItalyFamilyTreeDNA
KY409776SardiniansOlivieri 2017

I7

Haplogroup I7
Possible time of originAbout 9,100 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI
Defining mutationsC3534T, A4829G, T16324C

It is the rarest defined subclade, until July 2013 found only in two samples from the Near East and the Caucasus (Olivieri 2013).

GenBank IDPopulationSource
JF298212ArmenianFamilyTreeDNA
KF146253KuwaitOlivieri 2013

See also

Genetics

Backbone mtDNA Tree

Phylogenetic tree of human mitochondrial DNA (mtDNA) haplogroups

  Mitochondrial Eve (L)    
L0 L1–6  
L1 L2   L3     L4 L5 L6
M N  
CZ D E G Q   O A S R   I W X Y
C Z B F R0   pre-JT   P   U
HV JT K
H V J T

References

  1. Non, Amy. "ANALYSES OF GENETIC DATA WITHIN AN INTERDISCIPLINARY FRAMEWORK TO INVESTIGATE RECENT HUMAN EVOLUTIONARY HISTORY AND COMPLEX DISEASE" (PDF). University of Florida. Retrieved 12 April 2016.
  2. Rabab Khairat; Markus Ball; Chun-Chi Hsieh Chang; Raffaella Bianucci; Andreas G. Nerlich; Martin Trautmann; Somaia Ismail; et al. (4 April 2013). "First insights into the metagenome of Egyptian mummies using next-generation sequencing". Journal of Applied Genetics. 54 (3): 309–325. doi:10.1007/s13353-013-0145-1. PMID 23553074. S2CID 5459033. Retrieved 8 June 2016.
  3. Schuenemann, Verena J.; et al. (2017). "Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods". Nature Communications. 8: 15694. Bibcode:2017NatCo...815694S. doi:10.1038/ncomms15694. PMC 5459999. PMID 28556824.
  4. Sirak, Kendra; Frenandes, Daniel; Novak, Mario; Van Gerven, Dennis; Pinhasi, Ron (2016). "Abstract Book of the IUAES Inter-Congress 2016 - A community divided? Revealing the community genome(s) of Medieval Kulubnarti using next- generation sequencing". Abstract Book of the Iuaes Inter-Congress 2016. IUAES: 115–116.

Footnotes

  1. Nikitin 2009: 6/53 in Lemkos
    "Lemkos shared the highest frequency of haplogroup I ever reported and the highest frequency of haplogroup M* in the region."
  2. Cvjetan 2004: 15/133

Works cited

Journals

Books

  • Brook, Kevin Alan; Cooper, Leo R.; Wexler, Jeffrey D.; Lipson, Joshua; Stern, Jonah A. (2022). The Maternal Genetic Lineages of Ashkenazic Jews. Boston: Academic Studies Press. doi:10.2307/j.ctv33mgbcn. ISBN 978-1644699843. S2CID 254519342.

Websites

Further reading

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