Human diallelic insertion/deletion polymorphisms

Am J Hum Genet. 2002 Oct;71(4):854-62. doi: 10.1086/342727. Epub 2002 Sep 4.

Abstract

We report the identification and characterization of 2,000 human diallelic insertion/deletion polymorphisms (indels) distributed throughout the human genome. Candidate indels were identified by comparison of overlapping genomic or cDNA sequences. Average confirmation rate for indels with a > or =2-nt allele-length difference was 58%, but the confirmation rate for indels with a 1-nt length difference was only 14%. The vast majority of the human diallelic indels were monomorphic in chimpanzees and gorillas. The ratio of deletionrcolon;insertion mutations was 4.1. Allele frequencies for the indels were measured in Europeans, Africans, Japanese, and Native Americans. New alleles were generally lower in frequency than old alleles. This tendency was most pronounced for the Africans, who are likely to be closest among the four groups to the original modern human population. Diallelic indels comprise approximately 8% of all human polymorphisms. Their abundance and ease of analysis make them useful for many applications.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Biological Evolution*
  • Gene Deletion
  • Gene Frequency*
  • Genetics, Population
  • Humans
  • Mutagenesis, Insertional
  • Polymorphism, Genetic*