Database of Genomic Variants

URL:
http://projects.tcag.ca/variation/project.html
What you can do:
Find a comprehensive summary of structural variation in the human genome.
Highlights:
  • The objective of the Database of Genomic Variants is to provide a comprehensive summary of structural variation in the human genome. We define structural variation as genomic alterations that involve segments of DNA that are larger than >1kb. Now we also annotate InDels in 100bp-1kb range. The content of the database is only representing structural variation identified in healthy control samples.
  • The Database of Genomic Variants provides a useful catalog of control data for studies aiming to correlate genomic variation with phenotypic data. The database is continuously updated with new data from peer reviewed research studies. We always welcome suggestions and comments regarding the database from the research community.
Keywords:
  • structural variation
  • human genome
  • copy number variation
  • comparative genomic hybridization
  • CGH
  • FISH
  • CNVs
  • inversions
  • InDels
Literature & Tutorials:
PubMed Link: Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.
This record last updated: 10-25-2007
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