CNVVdb specifications


Unique identifier OMICS_22128
Name CNVVdb
Restrictions to use None
Community driven No
Data access File download, Browse
User data submission Not allowed


This tool is not maintained anymore.

Additional information

Publication for CNVVdb

CNVVdb citations


A classification model for distinguishing copy number variants from cancer related alterations

BMC Bioinformatics
PMCID: 2897829
PMID: 20525196
DOI: 10.1186/1471-2105-11-297

[…] on, smaller CNVs are less likely to be included into the DGV since they are detected less frequently in older, low-resolution arrays.There are other resources available that contain CNVs, for example CNVVdb (, DECIPHER (, 1000 genomes project ( and dbVAR ( […]


Gene Family Size Conservation Is a Good Indicator of Evolutionary Rates

Mol Biol Evol
PMCID: 2908708
PMID: 20194423
DOI: 10.1093/molbev/msq055

[…] g genes that have not been annotated by Ensembl, we downloaded all the genomic regions that were alignable with Ensembl-annotated protein-coding genes in the same-species self-chained alignments from CNVVdb () at Subsequently, all the protein isoforms of each Ensembl gene were aligned against these sequences using the BLAT protein-to-DNA alignment package (). […]

CNVVdb institution(s)
Division of Biostatistics and Bioinformatics, Institute of Population Health Sciences, National Health Research Institutes, Miaoli County, Taiwan; Genomics Research Center, Academia Sinica, Taipei, Taiwan
CNVVdb funding source(s)
Supported by the National Health Research Institutes (NHRI), Taiwan (NHRI-EX98-9408PC); National Science Council, Taiwan (NSC 96-2628-B-001-005-MY3); NHRI intramural funding.

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