A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652660



Internal ID15389312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56494872..56519496hg38UCSC Ensembl
Innerchr2:56722007..56746631hg19UCSC Ensembl
Innerchr2:56575511..56600135hg18UCSC Ensembl
Innerchr2:56633658..56658282hg17UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3824625
hg1924625
hg1824625
hg1724625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517645
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652660
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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