A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10520n54



Internal ID22778415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32504326..32517715hg38UCSC Ensembl
chr6:32472103..32485492hg19UCSC Ensembl
chr6:32580081..32593470hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3813390
hg1913390
hg1813390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602352, nsv602353, nsv602355, nsv602369, nsv602368, nsv602348
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10520n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss69
Observed Complex0
Frequencyn/a


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