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Structural variation of the human genome

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

211 Scopus citations

Abstract

There is growing appreciation that the human genome contains significant numbers of structural rearrangements, such as insertions, deletions, inversions, and large tandem repeats. Recent studies have defined approximately 5% of the human genome as structurally variant in the normal population, involving more than 800 independent genes. We present a detailed review of the various structural rearrangements identified to date in humans, with particular reference to their influence on human phenotypic variation. Our current knowledge of the extent of human structural variation shows that the human genome is a highly dynamic structure that shows significant large-scale variation from the currently published genome reference sequence.

Original languageEnglish
Title of host publicationAnnual Review of Genomics and Human Genetics
EditorsAravinda Chakravarti, Eric Green
Pages407-442
Number of pages36
DOIs
StatePublished - 2006
Externally publishedYes

Publication series

NameAnnual Review of Genomics and Human Genetics
Volume7
ISSN (Print)1527-8204

Keywords

  • Deletion
  • Insertion
  • Inversion
  • Polymorphism
  • Rearrangement

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