A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806762



Internal ID15754032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23197675..24374789hg38UCSC Ensembl
Innerchr13:23771814..24948927hg19UCSC Ensembl
Innerchr13:22669814..23846927hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381177115
hg191177114
hg181177114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561332
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)nssv806762
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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