A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713237



Internal ID19011518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70263815..70399170hg38UCSC Ensembl
Innerchr13:70837947..70973302hg19UCSC Ensembl
Innerchr13:69735948..69871303hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38135356
hg19135356
hg18135356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037421
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)nssv3713237
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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