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Resource Name
Leiden Open Variation Database
RRID:SCR_006566 RRID Copied      
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Leiden Open Variation Database (RRID:SCR_006566)
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Resource Information

URL: http://www.LOVD.nl/

Proper Citation: Leiden Open Variation Database (RRID:SCR_006566)

Description: Freely available tool for Gene-centered collection and display of DNA variations. It also provides patient-centered data storage and storage of Next Generation Sequencing (NGS) data, even of variants outside of genes. Please note that LOVD provides a system for storage of information on genes and allelic variants. To obtain information about any genes or variants, do not download the LOVD package. This information should be obtained from the respective databases, http://www.lovd.nl/2.0/index_list.php In total: 2,507,027 variants (2,208,937 unique) in 170,935 individuals in 62619 genes in 88 LOVD installations. (Aug. 2013) LOVD 3.0 shared installation, http://databases.lovd.nl/shared/genes To maintain a high quality of the data stored, LOVD connects with various resources, like HGNC, NCBI, EBI and Mutalyzer. You can download LOVD in ZIP and GZIPped TARball formats.

Abbreviations: LOVD

Synonyms: Leiden Open Variation Database (LOVD)

Resource Type: data or information resource, data storage software, service resource, database, storage service resource, software resource, data repository, software application, data processing software

Defining Citation: PMID:21520333, PMID:15977173

Keywords: genetic variation, genomic variant, gene, transcript, disease, next generation sequencing, dna variation, variant, clinical, screening, locus, phenotype, sequence variation, allelic variant, data sharing, FASEB list

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Leiden University; Leiden; Netherlands

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