A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791937



Internal ID19160125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78720790..78999525hg38UCSC Ensembl
Innerchr16:78754687..79033422hg19UCSC Ensembl
Innerchr16:77312188..77590923hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38278736
hg19278736
hg18278736
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892908
Supporting Variants
Samples
Known GenesWWOX
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=150
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791937
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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