CNV DB specifications


Unique identifier OMICS_22119
Alternative name Copy Number Variation Database
Restrictions to use None
Community driven No
Data access Browse
User data submission Not allowed
Maintained Yes

CNV DB citation


Comparison of solution based exome capture methods for next generation sequencing

Genome Biol
PMCID: 3308057
PMID: 21955854
DOI: 10.1186/gb-2011-12-9-r94

[…] pture methods shared 27 REAs and NimbleGen's methods shared 19 REAs. Of the indels identified with pileup, 30% overlapped with known indels from dbSNP b130 and 43% of the REAs overlapped with a known copy number variation (Database of Genomic Variants, March 2010 freeze). Extensive validation of the found indels is needed for the evaluation of the algorithms. […]

CNV DB funding source(s)
Supported by Ministry of Education, Culture, Sports, Science and Technology of Japan.

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