A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156643



Internal ID15877539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131753494..131815815hg38UCSC Ensembl
Innerchr8:132765741..132828062hg19UCSC Ensembl
Innerchr8:132834923..132897244hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3862322
hg1962322
hg1862322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612324
Supporting Variants
SamplesHGDP01004
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156643
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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