A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004959



Internal ID7070055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56888436..56888913hg38UCSC Ensembl
Innerchr17:54965797..54966274hg19UCSC Ensembl
Innerchr17:52320796..52321273hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38478
hg19478
hg18478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587003
SamplesHuRef
Known GenesTRIM25
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004959
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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