A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602730



Internal ID16043453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32641404..32641650hg38UCSC Ensembl
Innerchr6:32609181..32609427hg19UCSC Ensembl
Innerchr6:32717159..32717405hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38247
hg19247
hg18247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1056590, nssv1056588, nssv1056589
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602730
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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