A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990867



Internal ID7076998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38714155..38715151hg38UCSC Ensembl
Innerchr15:39006356..39007352hg19UCSC Ensembl
Innerchr15:36793648..36794644hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38997
hg19997
hg18997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586406
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990867
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