A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602732



Internal ID16390141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32641404..32643864hg38UCSC Ensembl
Innerchr6:32609181..32611641hg19UCSC Ensembl
Innerchr6:32717159..32719619hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382461
hg192461
hg182461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10590n54
Supporting Variantsnssv1056598, nssv1056597
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602732
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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