A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586370



Internal ID6711066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73969007..73973406hg38UCSC Ensembl
Innerchr11:73680052..73684451hg19UCSC Ensembl
Innerchr11:73357700..73362099hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384400
hg194400
hg184400
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001380
Supporting Variants
SamplesHuRef
Known GenesDNAJB13
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586370
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