Leiden Open Variation Database 3.0

Directly see all databases of your gene of interest from our LSDB list:
Examples: DMD.lovd.nl, BRCA1.lovd.nl.

LOVD stands for Leiden Open (source) Variation Database.
LOVD's purpose : To provide a flexible, freely available tool for genomic variant and phenotype collection, display and curation. LOVD allows both patient-centered and gene-centered views. LOVD is open source, released under the GPL license, and is actively being improved. On the server in Leiden, LOVD offers free hosting and support of LOVD-powered gene variant databases.

To maintain a high quality of the data stored, LOVD connects with various resources, like HGNC, NCBI, EBI and Mutalyzer.

LOVD 3.0 is the successor of LOVD 2.0. Do you want to know more about the changes between LOVD 2.0 and 3.0?
Want to see what LOVD 3.0 looks like?

LOVD features integration with the Mutalyzer sequence variant nomenclature checker, allowing for direct nomenclature checking of sequence variants during the submission process.

Last modified 2019/12/18 12:54:42 CET

When using or discussing LOVD please refer to:
Fokkema IF, Kroon M, López Hernández JA, Asscheman D, Lugtenburg I, Hoogenboom J, den Dunnen JT. The LOVD3 platform: efficient genome-wide sharing of genetic variants. Eur J Hum Genet (2021). https://doi.org/10.1038/s41431-021-00959-x.

A recommended system of the Human Variome Project LOVD has received funding from the European Community's Seventh Framework Programme
(FP7/2007-2013) under grant agreement nº 200754 - the GEN2PHEN project.
©2004-2021 Leiden University Medical Center, Netherlands
Ivo F.A.C. Fokkema BSc., Prof. Johan T. den Dunnen PhD
A IRDiRC recognized resource