Name any two variants found in human
populations.
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22
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Genetic variations in the human genome can take many forms, including single nucleotide changes or substitutions; tandem repeats; insertions and deletions (indels); additions or deletions that change the copies number of a larger segment of DNA sequence; that is, copy number variations (CNVs); other chromosomal ..
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Structural variations, such as copy-number variation and deletions, inversions, insertions and duplications, account for much more human genetic variation than single nucleotide diversity.
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