A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610775



Internal ID16051498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23080343..23139266hg38UCSC Ensembl
Innerchr8:22937856..22996779hg19UCSC Ensembl
Innerchr8:22993801..23052724hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3858924
hg1958924
hg1858924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107479
Samples
Known GenesLOC254896, LOC286059, TNFRSF10C, TNFRSF10D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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