A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725964



Internal ID19024245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36123960..36341979hg38UCSC Ensembl
Innerchr2:36351103..36569122hg19UCSC Ensembl
Innerchr2:36204607..36422626hg18UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38218020
hg19218020
hg18218020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004156
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3725964
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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