A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523157



Internal ID18821438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23645821..23913651hg38UCSC Ensembl
Innerchr13:24219960..24487790hg19UCSC Ensembl
Innerchr13:23117960..23385790hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38267831
hg19267831
hg18267831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041095
Supporting Variants
Samples
Known GenesANKRD20A19P, C1QTNF9B, C1QTNF9B-AS1, MIPEP, TNFRSF19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523157
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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