A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010097



Internal ID7074162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37416900..37421619hg38UCSC Ensembl
Innerchr17:35776985..35781702hg19UCSC Ensembl
Innerchr17:32851098..32855815hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384720
hg194718
hg184718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587121
SamplesHuRef
Known GenesTADA2A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010097
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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