A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993199



Internal ID7078532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134882287..134886809hg38UCSC Ensembl
Innerchr8:135894530..135899052hg19UCSC Ensembl
Innerchr8:135963712..135968234hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg384523
hg194523
hg184523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586432
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993199
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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