A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10586n54



Internal ID22778481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32625121..32811865hg38UCSC Ensembl
chr6:32592898..32779642hg19UCSC Ensembl
chr6:32700876..32887620hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38186745
hg19186745
hg18186745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602744, nsv602768, nsv602740, nsv602709, nsv602715, nsv602723, nsv602735
Samples
Known GenesHLA-DQA1, HLA-DQA2, HLA-DQB1, HLA-DQB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10586n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss51
Observed Complex0
Frequencyn/a


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