A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602236



Internal ID16389645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491063..32598517hg38UCSC Ensembl
Innerchr6:32458840..32566294hg19UCSC Ensembl
Innerchr6:32566818..32674272hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38107455
hg19107455
hg18107455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10505n54
Supporting Variantsnssv1054655
Samples
Known GenesHLA-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)nsv602236
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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