A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610176



Internal ID16397585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8461340..8593251hg38UCSC Ensembl
Innerchr8:8318850..8450761hg19UCSC Ensembl
Innerchr8:8356260..8488171hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38131912
hg19131912
hg18131912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11939n54
Supporting Variantsnssv1156581, nssv1156582
SamplesHGDP01234, HGDP01215
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610176
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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