A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10504n54



Internal ID22778399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32487705..32598517hg38UCSC Ensembl
chr6:32455482..32566294hg19UCSC Ensembl
chr6:32563460..32674272hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38110813
hg19110813
hg18110813
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602273, nsv602176, nsv602267, nsv602182
Samples
Known GenesHLA-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)dgv10504n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss19
Observed Complex0
Frequencyn/a


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