A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806246



Internal ID15753516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23025847..24348376hg38UCSC Ensembl
Innerchr13:23599986..24922514hg19UCSC Ensembl
Innerchr13:22497986..23820514hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381322530
hg191322529
hg181322529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561292
Supporting Variants
Samples
Known GenesANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv806246
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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