A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10558n54



Internal ID22778453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32556447..32604329hg38UCSC Ensembl
chr6:32524224..32572106hg19UCSC Ensembl
chr6:32632202..32680084hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3847883
hg1947883
hg1847883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602554, nsv602576, nsv602572, nsv602565, nsv602553
Samples
Known GenesHLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10558n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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