A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611644



Internal ID16399053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83616035..83648108hg38UCSC Ensembl
Innerchr8:84528270..84560343hg19UCSC Ensembl
Innerchr8:84690825..84722898hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3832074
hg1932074
hg1832074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12221n54
Supporting Variantsnssv1156627
SamplesHGDP00141
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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