A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10599n54



Internal ID22778494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32659261..32685658hg38UCSC Ensembl
chr6:32627038..32653435hg19UCSC Ensembl
chr6:32735016..32761413hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826398
hg1926398
hg1826398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602783, nsv602785
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10599n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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