A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991936



Internal ID7077610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19707241..19707941hg38UCSC Ensembl
Innerchr16:19718563..19719263hg19UCSC Ensembl
Innerchr16:19626064..19626764hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38701
hg19701
hg18701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586923
SamplesHuRef
Known GenesKNOP1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991936
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer