A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10529n54



Internal ID22778424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32519533..32666554hg38UCSC Ensembl
chr6:32487310..32634331hg19UCSC Ensembl
chr6:32595288..32742309hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38147022
hg19147022
hg18147022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602462, nsv602559, nsv602510, nsv602482, nsv602545, nsv602556, nsv602526, nsv602417, nsv602409, nsv602425
Samples
Known GenesHLA-DQA1, HLA-DQB1, HLA-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)dgv10529n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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