A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156626



Internal ID15877031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83616035..83647386hg38UCSC Ensembl
Innerchr8:84528270..84559621hg19UCSC Ensembl
Innerchr8:84690825..84722176hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3831352
hg1931352
hg1831352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611643
Supporting Variants
SamplesHGDP00926
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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