A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586786



Internal ID7058168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32482722..32559154hg38UCSC Ensembl
Innerchr6:32450499..32526931hg19UCSC Ensembl
Innerchr6:32558477..32634909hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3876433
hg1976433
hg1876433
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007504
Supporting Variants
SamplesHuRef
Known GenesHLA-DRB5, HLA-DRB6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586786
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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