A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10518n54



Internal ID22778413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32501123..32524531hg38UCSC Ensembl
chr6:32468900..32492308hg19UCSC Ensembl
chr6:32576878..32600286hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3823409
hg1923409
hg1823409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602370, nsv602333, nsv602360, nsv602341
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10518n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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