A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602693



Internal ID16390102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32609603..32701379hg38UCSC Ensembl
Innerchr6:32577380..32669156hg19UCSC Ensembl
Innerchr6:32685358..32777134hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3891777
hg1991777
hg1891777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1056406
Samples
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)nsv602693
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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