A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054652



Internal ID15907838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491063..32592485hg38UCSC Ensembl
Innerchr6:32458840..32560262hg19UCSC Ensembl
Innerchr6:32566818..32668240hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38101423
hg19101423
hg18101423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602233
Supporting Variants
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)nssv1054652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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