A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10585n54



Internal ID22778480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32625121..32644620hg38UCSC Ensembl
chr6:32592898..32612397hg19UCSC Ensembl
chr6:32700876..32720375hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3819500
hg1919500
hg1819500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602703, nsv602702, nsv602704
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10585n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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