A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788187



Internal ID19172728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78369011..78982511hg38UCSC Ensembl
Innerchr16:78402908..79016408hg19UCSC Ensembl
Innerchr16:76960409..77573909hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38613501
hg19613501
hg18613501
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892903
Supporting Variants
Samples
Known GenesWWOX
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=304
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788187
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer