A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10591n54



Internal ID22778486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32641154..32663681hg38UCSC Ensembl
chr6:32608931..32631458hg19UCSC Ensembl
chr6:32716909..32739436hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3822528
hg1922528
hg1822528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602727, nsv602764, nsv602736, nsv602757, nsv602763, nsv602765, nsv602722, nsv602742, nsv602733, nsv602729, nsv602726, nsv602728, nsv602755, nsv602739, nsv602721, nsv602734
Samples
Known GenesHLA-DQA1, HLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10591n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss63
Observed Complex0
Frequencyn/a


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