A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10514n54



Internal ID22778409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32498382..32575763hg38UCSC Ensembl
chr6:32466159..32543540hg19UCSC Ensembl
chr6:32574137..32651518hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3877382
hg1977382
hg1877382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602324, nsv602322, nsv602323, nsv602321
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)dgv10514n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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