A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586675



Internal ID7058057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1914470..1915765hg38UCSC Ensembl
Innerchr20:1895116..1896411hg19UCSC Ensembl
Innerchr20:1843116..1844411hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381296
hg191296
hg181296
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005896
Supporting Variants
SamplesHuRef
Known GenesSIRPA
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586675
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