A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999877



Internal ID7082485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32533542..32570584hg38UCSC Ensembl
Innerchr6:32501319..32538361hg19UCSC Ensembl
Innerchr6:32609297..32646339hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3837043
hg1937043
hg1837043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586741
SamplesHuRef
Known GenesHLA-DRB6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999877
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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