A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611710



Internal ID16399119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86801299..86844234hg38UCSC Ensembl
Innerchr8:87813527..87856462hg19UCSC Ensembl
Innerchr8:87882643..87925578hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3842936
hg1942936
hg1842936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117705
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611710
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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