A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997323



Internal ID7081293
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586313
SamplesHuRef
Known GenesOR51B5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997323
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