A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10584n54



Internal ID22778479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32625074..32663681hg38UCSC Ensembl
chr6:32592851..32631458hg19UCSC Ensembl
chr6:32700829..32739436hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3838608
hg1938608
hg1838608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602699, nsv602708, nsv602707, nsv602705, nsv602706
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)dgv10584n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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