A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586987



Internal ID7058369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74452828..74454726hg38UCSC Ensembl
Innerchr8:75365063..75366961hg19UCSC Ensembl
Innerchr8:75527618..75529516hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007964
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586987
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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