A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602643



Internal ID16390052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32581949..32658092hg38UCSC Ensembl
Innerchr6:32549726..32625869hg19UCSC Ensembl
Innerchr6:32657704..32733847hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3876144
hg1976144
hg1876144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10563n54
Supporting Variantsnssv1056302
Samples
Known GenesHLA-DQA1, HLA-DRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602643
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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