A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156656



Internal ID15530509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143021076..143084012hg38UCSC Ensembl
Innerchr8:144102493..144165429hg19UCSC Ensembl
Innerchr8:144173868..144236804hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3862937
hg1962937
hg1862937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612717
Supporting Variants
SamplesHGDP00949
Known GenesC8orf31, LY6E
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156656
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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