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Chromosome 12 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 12 spans about 133 million base pairs (the building material of DNA) and represents between 4 and 4.5 percent of the total DNA in cells. Chromosome 12 contains the Homeobox C gene cluster.
Chromosome 1 spans about 249 million nucleotide base pairs, which are the basic units of information for DNA. [4] It represents about 8% of the total DNA in human cells. [5] It was the last completed chromosome, sequenced two decades after the beginning of the Human Genome Project.
Chromosome 13 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 13 spans about 113 million base pairs (the building material of DNA ) and represents between 3.5 and 4% of the total DNA in cells .
[26] [10] As more progress has been made on sequencing the human genome, it has been found that any two humans will share an average of 99.35% of their DNA based on the approximately 3.1 billion haploid base pairs.
An allele [1] (or allelomorph) is a variant of the sequence of nucleotides at a particular location, or locus, on a DNA molecule. [2]Alleles can differ at a single position through single nucleotide polymorphisms (SNP), [3] but they can also have insertions and deletions of up to several thousand base pairs.
Haplogroup Q or Q-M242 is a Y-chromosome DNA haplogroup. It has one primary subclade, Haplogroup Q1 (L232/S432), which includes numerous subclades that have been sampled and identified in males among modern populations. Q-M242 is the predominant Y-DNA haplogroup among Native Americans, Swati tribe and several peoples of Central Asia and ...
In human genetics, Haplogroup J-M172 or J2 [Phylogenetics 1] is a Y-chromosome haplogroup which is a subclade (branch) of haplogroup J-M304. [Phylogenetics 2] Haplogroup J-M172 is common in modern populations in Western Asia, Central Asia, South Asia, Southern Europe, Northwestern Iran and North Africa.
A measure of inbreeding of an individual A is the probability F(A) that both alleles in one locus are derived from the same allele in an ancestor. These two identical alleles that are both derived from a common ancestor are said to be identical by descent. This probability F(A) is called the "coefficient of inbreeding". [43]