A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10597n54



Internal ID22778492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32651877..32659936hg38UCSC Ensembl
chr6:32619654..32627713hg19UCSC Ensembl
chr6:32727632..32735691hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388060
hg198060
hg188060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602773, nsv602772
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10597n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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