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Database of Genomic Variants DGV

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Provides 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 50bp. 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.

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DGV classification

  • Animals
    • Homo sapiens

DGV specifications

Restrictions to use:
None
Maintained:
Yes

DGV distribution

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Publications

Institution(s)

The Centre for Applied Genomics, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada

Link to literature

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