10-02-2023, 04:46 PM
I thought a thread about one of the more commonly seen mtDNA would be interesting and helpful. Any comments or thoughts would be greatly appreciated.
According to the H1 mtDNA Full Genomic Sequence (mtGenome) Project at FTDNA:
Unlike other branches of the mega-haplogroup H, the defining mutation for H1 (3010A) has likely happened many times in the history of H. This recurrent nature of H1 adds an extra layer of complexity to understanding our direct maternal origins within H1 and its sub-branches.
H1 encompasses an important fraction of Western European mtDNA, reaching its local peak among contemporary Basques and appearing at a high frequency among other Iberians and North Africans. Its frequency is above 10% in many other parts of Europe (France, Sardinia, British Isles, Alps, large portions of Eastern Europe), and above 5% in nearly all the continent. Its subclade H1b is most common in eastern Europe and NW Siberia.] So far, the highest frequency of H1 - 61%- has been found among the Tuareg of the Fezzan region in .Libya.
Eupedia has the following about H1:
Haplogroup H1 is by far the most common subclade in Europe, representing approximately than half of the H lineages in Western Europe. Roostalu et al. (2006) estimate that H1 arose around 22,500 years ago. H1 is divided in 65 basal subclades. The largest, H1c, has over 20 more basal subclades of its own, most with deeper ramifications. H1 is found throughout Europe, North Africa, the Levant, Anatolia, the Caucasus, and as far as Central Asia and Siberia. The highest frequencies of H1 are observed in the Iberian peninsula, south-west France and Sardinia.
Being that my mtDNA is H1c, I have the following TMRCA for H1 and and H1c and some of its branches from YFull.
According to the H1 mtDNA Full Genomic Sequence (mtGenome) Project at FTDNA:
Unlike other branches of the mega-haplogroup H, the defining mutation for H1 (3010A) has likely happened many times in the history of H. This recurrent nature of H1 adds an extra layer of complexity to understanding our direct maternal origins within H1 and its sub-branches.
H1 encompasses an important fraction of Western European mtDNA, reaching its local peak among contemporary Basques and appearing at a high frequency among other Iberians and North Africans. Its frequency is above 10% in many other parts of Europe (France, Sardinia, British Isles, Alps, large portions of Eastern Europe), and above 5% in nearly all the continent. Its subclade H1b is most common in eastern Europe and NW Siberia.] So far, the highest frequency of H1 - 61%- has been found among the Tuareg of the Fezzan region in .Libya.
Eupedia has the following about H1:
Haplogroup H1 is by far the most common subclade in Europe, representing approximately than half of the H lineages in Western Europe. Roostalu et al. (2006) estimate that H1 arose around 22,500 years ago. H1 is divided in 65 basal subclades. The largest, H1c, has over 20 more basal subclades of its own, most with deeper ramifications. H1 is found throughout Europe, North Africa, the Levant, Anatolia, the Caucasus, and as far as Central Asia and Siberia. The highest frequencies of H1 are observed in the Iberian peninsula, south-west France and Sardinia.
Being that my mtDNA is H1c, I have the following TMRCA for H1 and and H1c and some of its branches from YFull.