A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611632



Internal ID16399041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83211843..83307039hg38UCSC Ensembl
Innerchr8:84124078..84219274hg19UCSC Ensembl
Innerchr8:84286633..84381829hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3895197
hg1995197
hg1895197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117327
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611632
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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