A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892903



Internal ID19183723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78369011..78982511hg38UCSC Ensembl
Outerchr16:78369011..78982511hg38UCSC Ensembl
Innerchr16:78402908..79016408hg19UCSC Ensembl
Outerchr16:78402908..79016408hg19UCSC Ensembl
Innerchr16:76960409..77573909hg18UCSC Ensembl
Outerchr16:76960409..77573909hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38613501
hg19613501
hg18613501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788187
Samples
Known GenesWWOX
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892903
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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