A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10582n54



Internal ID22778477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32610275..32687441hg38UCSC Ensembl
chr6:32578052..32655218hg19UCSC Ensembl
chr6:32686030..32763196hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3877167
hg1977167
hg1877167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602697, nsv602695, nsv602694
SamplesHGDP00546, HGDP00606, HGDP00737
Known GenesHLA-DQA1, HLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10582n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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