A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586313



Internal ID7057695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5361555..5362700hg38UCSC Ensembl
Innerchr11:5382785..5383930hg19UCSC Ensembl
Innerchr11:5339361..5340506hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381146
hg191146
hg181146
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997323
Supporting Variants
SamplesHuRef
Known GenesOR51B5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586313
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