A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156578



Internal ID15877318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8455500..8593251hg38UCSC Ensembl
Innerchr8:8313010..8450761hg19UCSC Ensembl
Innerchr8:8350420..8488171hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38137752
hg19137752
hg18137752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610173
Supporting Variants
SamplesHGDP00967
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156578
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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