A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999114



Internal ID7064750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79151285..79152314hg38UCSC Ensembl
Innerchr16:79185182..79186211hg19UCSC Ensembl
Innerchr16:77742683..77743712hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381030
hg191030
hg181030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586194
SamplesHuRef
Known GenesWWOX
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999114
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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