A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602358



Internal ID16389767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32505132..32685658hg38UCSC Ensembl
Innerchr6:32472909..32653435hg19UCSC Ensembl
Innerchr6:32580887..32761413hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38180527
hg19180527
hg18180527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10489n54
Supporting Variantsnssv1055230
Samples
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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