A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176054



Internal ID15854034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63395129..63430950hg38UCSC Ensembl
Innerchr13:63969262..64005083hg19UCSC Ensembl
Innerchr13:62867263..62903084hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3835822
hg1935822
hg1835822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561903
Supporting Variants
Samples1780854536_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176054
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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