A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007964



Internal ID7073057
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586987
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007964
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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