A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580884



Internal ID18879165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34001289..34092762hg38UCSC Ensembl
Innerchr2:34226356..34317829hg19UCSC Ensembl
Innerchr2:34079860..34171333hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3891474
hg1991474
hg1891474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012223
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)nssv3580884
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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