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PMID: 12205564 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Human diallelic insertion/deletion polymorphisms.

American journal of human genetics ·Vol. 71 ·No. 4 ·2002-10-00 ·Pages 854-62

Weber JL, David D, Heil J, Fan Y, Zhao C, Marth G

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.

MeSH Terms
Biological Evolution Gene Deletion Gene Frequency Genetics, Population Humans Mutagenesis, Insertional Polymorphism, Genetic
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Weber James L
Center for Medical Genetics, Marshfield Medical Research Foundation, Marshfield, WI 54449, USA. weberj@cmg.mfldclin.edu
David Donna
Heil Jeremy
Fan Ying
Zhao Chengfeng
Marth Gabor
References (26)
26 references, click to expand
  1. A general approach to single-nucleotide polymorphism discovery.
    Nat Genet. 1999 Dec;23(4):452-6 PMID: 10581034
  2. Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.
    Nat Genet. 1999 Jun;22(2):164-7 PMID: 10369258
  3. Human BAC ends quality assessment and sequence analyses.
    Genomics. 2000 Feb 1;63(3):321-32 PMID: 10704280
  4. Microsatellites in different eukaryotic genomes: survey and analysis.
    Genome Res. 2000 Jul;10(7):967-81 PMID: 10899146
  5. Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.
    Am J Hum Genet. 2000 Oct;67(4):901-25 PMID: 10986042
  6. Analysis of the genome sequence of the flowering plant Arabidopsis thaliana.
    Nature. 2000 Dec 14;408(6814):796-815 PMID: 11130711
  7. A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence.
    Genome Res. 2001 Jan;11(1):170-8 PMID: 11156626
  8. Disease-causing mutations in the human genome.
    Eur J Pediatr. 2000 Dec;159 Suppl 3:S173-8 PMID: 11216894
  9. Patterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphisms.
    Am J Hum Genet. 2001 Mar;68(3):738-52 PMID: 11179020
  10. Great ape DNA sequences reveal a reduced diversity and an expansion in humans.
    Nat Genet. 2001 Feb;27(2):155-6 PMID: 11175781
  11. Regions of low single-nucleotide polymorphism incidence in human and orangutan xq: deserts and recent coalescences.
    Genomics. 2001 Jan 1;71(1):78-88 PMID: 11161800
  12. Initial sequencing and analysis of the human genome.
    Nature. 2001 Feb 15;409(6822):860-921 PMID: 11237011
  13. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.
    Nature. 2001 Feb 15;409(6822):928-33 PMID: 11237013
  14. Single-nucleotide polymorphisms in the public domain: how useful are they?
    Nat Genet. 2001 Apr;27(4):371-2 PMID: 11279516
  15. Rapid gene mapping in Caenorhabditis elegans using a high density polymorphism map.
    Nat Genet. 2001 Jun;28(2):160-4 PMID: 11381264
  16. Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity.
    Environ Mol Mutagen. 2001;37(4):311-23 PMID: 11424181
  17. Sequence variation and linkage disequilibrium in the human T-cell receptor beta (TCRB) locus.
    Am J Hum Genet. 2001 Aug;69(2):381-95 PMID: 11438886
  18. Population genomics: a bridge from evolutionary history to genetic medicine.
    Hum Mol Genet. 2001 Oct 1;10(20):2199-207 PMID: 11673402
  19. Genetic mapping with SNP markers in Drosophila.
    Nat Genet. 2001 Dec;29(4):475-81 PMID: 11726933
  20. Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment.
    Hum Genet. 1991 Mar;86(5):425-41 PMID: 2016084
  21. Mechanisms of insertional mutagenesis in human genes causing genetic disease.
    Hum Genet. 1991 Aug;87(4):409-15 PMID: 1652548
  22. Statistical properties of segregating sites.
    Theor Popul Biol. 1995 Oct;48(2):172-97 PMID: 7482370
  23. Chromosomal duplications in bacteria, fruit flies, and humans.
    Am J Hum Genet. 1996 Jan;58(1):21-7 PMID: 8554058
  24. Neutral behavior of shared polymorphism.
    Proc Natl Acad Sci U S A. 1997 Jul 22;94(15):7730-4 PMID: 9223256
  25. A DNA polymorphism discovery resource for research on human genetic variation.
    Genome Res. 1998 Dec;8(12):1229-31 PMID: 9872978
  26. Use of molecular variation in the NCBI dbSNP database.
    Hum Mutat. 2000;15(1):68-75 PMID: 10612825
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
2002-10-00
Epub
2002-00-04
Pages
854-62
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC378541
Subset
IM
Grants
NHLBI NIH HHS · N01HV48141 · United States
NHLBI NIH HHS · HL62681 · United States
NHLBI NIH HHS · HV48141 · United States
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