A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610566



Internal ID16397975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15859387..15964860hg38UCSC Ensembl
Innerchr8:15716896..15822369hg19UCSC Ensembl
Innerchr8:15761267..15866740hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38105474
hg19105474
hg18105474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106946
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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