A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892905



Internal ID19183725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78471101..78687864hg38UCSC Ensembl
Outerchr16:78471101..78687864hg38UCSC Ensembl
Innerchr16:78504998..78721761hg19UCSC Ensembl
Outerchr16:78504998..78721761hg19UCSC Ensembl
Innerchr16:77062499..77279262hg18UCSC Ensembl
Outerchr16:77062499..77279262hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38216764
hg19216764
hg18216764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786088
Samples
Known GenesWWOX
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892905
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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