A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587003



Internal ID7058385
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004959
Supporting Variants
SamplesHuRef
Known GenesTRIM25
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587003
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer