A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602694



Internal ID16390103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32610275..32684540hg38UCSC Ensembl
Innerchr6:32578052..32652317hg19UCSC Ensembl
Innerchr6:32686030..32760295hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3874266
hg1974266
hg1874266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10582n54
Supporting Variantsnssv1154739
SamplesHGDP00737
Known GenesHLA-DQA1, HLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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