A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10589n54



Internal ID22778484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32641154..32643220hg38UCSC Ensembl
chr6:32608931..32610997hg19UCSC Ensembl
chr6:32716909..32718975hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382067
hg192067
hg182067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602731, nsv602719, nsv602725, nsv602724, nsv602718
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10589n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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