A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10600n54



Internal ID22778495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32660181..32666628hg38UCSC Ensembl
chr6:32627958..32634405hg19UCSC Ensembl
chr6:32735936..32742383hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386448
hg196448
hg186448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602784, nsv602786
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10600n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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