A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009065



Internal ID7059111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152459134..152466790hg38UCSC Ensembl
Innerchr5:151838695..151846351hg19UCSC Ensembl
Innerchr5:151818888..151826544hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg387657
hg197657
hg187657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586544
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009065
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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