A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892902



Internal ID18837036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78049580..78674801hg38UCSC Ensembl
Outerchr16:78049580..78674801hg38UCSC Ensembl
Innerchr16:78083477..78708698hg19UCSC Ensembl
Outerchr16:78083477..78708698hg19UCSC Ensembl
Innerchr16:76640978..77266199hg18UCSC Ensembl
Outerchr16:76640978..77266199hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38625222
hg19625222
hg18625222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788381
Samples
Known GenesWWOX
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892902
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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