A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998282



Internal ID7081685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31356709..31359968hg38UCSC Ensembl
Innerchr6:31324486..31327745hg19UCSC Ensembl
Innerchr6:31432465..31435724hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383260
hg193260
hg183260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586152
SamplesHuRef
Known GenesHLA-B
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998282
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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