A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1109987



Internal ID15963173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:33792338..33958454hg38UCSC Ensembl
Innerchr8:33649856..33815972hg19UCSC Ensembl
Innerchr8:33769398..33935514hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38166117
hg19166117
hg18166117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610930
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1109987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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