A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726746



Internal ID19025027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12432821..12451569hg38UCSC Ensembl
Innerchr2:12572947..12591695hg19UCSC Ensembl
Innerchr2:12490398..12509146hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3818749
hg1918749
hg1818749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005438
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)nssv3726746
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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