A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10522n54



Internal ID22778417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32504326..32568117hg38UCSC Ensembl
chr6:32472103..32535894hg19UCSC Ensembl
chr6:32580081..32643872hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3863792
hg1963792
hg1863792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602350, nsv602386, nsv602385, nsv602403, nsv602388, nsv602362, nsv602387
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10522n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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