A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602215



Internal ID16389624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32490550..32582653hg38UCSC Ensembl
Innerchr6:32458327..32550430hg19UCSC Ensembl
Innerchr6:32566305..32658408hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3892104
hg1992104
hg1892104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054604
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)nsv602215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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