A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10502n54



Internal ID22778397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32487705..32546367hg38UCSC Ensembl
chr6:32455482..32514144hg19UCSC Ensembl
chr6:32563460..32622122hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3858663
hg1958663
hg1858663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602164, nsv602169, nsv602254, nsv602163, nsv602312, nsv602206, nsv602255, nsv602166, nsv602165, nsv602207, nsv602205, nsv602167, nsv602168, nsv602310, nsv602302, nsv602204
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10502n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


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