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Leiden Open Variation Database LOVD

Online

Provide a flexible, freely available tool for Gene-centered collection and display of DNA variations. LOVD 3.0 extends this idea to also provide patient-centered data storage and storage of NGS data, even of variants outside of genes. LOVD allows users to link large numbers of DNA variants in one or more genes to an individual (multi-gene disorders or large scale next-generation sequencing). You can even use LOVD on your personal computer to browse through the variants in your own exome/genome. To maintain a high quality of the data stored, LOVD connects with various resources, like HGNC, NCBI, EBI and Mutalyzer.

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LOVD forum

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LOVD classification

  • Animals
    • Homo sapiens

LOVD specifications

Restrictions to use:
None
Maintained:
Yes
Version:
3.0

LOVD distribution

LOVD support

Maintainer

  • Peter E. M. Taschner <>

Credits

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Publications

Institution(s)

Center of Human and Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands

Link to literature

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