A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611427



Internal ID16398836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61820708..61936393hg38UCSC Ensembl
Innerchr8:62733267..62848952hg19UCSC Ensembl
Innerchr8:62895821..63011506hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38115686
hg19115686
hg18115686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115649
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611427
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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