A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992587



Internal ID7078148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100736422..100737196hg38UCSC Ensembl
Innerchr14:101202759..101203533hg19UCSC Ensembl
Innerchr14:100272512..100273286hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38775
hg19775
hg18775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587070
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992587
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