A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892908



Internal ID19183728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78720790..78999525hg38UCSC Ensembl
Outerchr16:78720790..78999525hg38UCSC Ensembl
Innerchr16:78754687..79033422hg19UCSC Ensembl
Outerchr16:78754687..79033422hg19UCSC Ensembl
Innerchr16:77312188..77590923hg18UCSC Ensembl
Outerchr16:77312188..77590923hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38278736
hg19278736
hg18278736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791937
Samples
Known GenesWWOX
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892908
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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