A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175922



Internal ID15534457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22937442..24341413hg38UCSC Ensembl
Innerchr13:23511581..24915551hg19UCSC Ensembl
Innerchr13:22409581..23813551hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381403972
hg191403971
hg181403971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561285
Supporting Variants
SamplesNINDS_72
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)nssv1175922
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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