A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116629



Internal ID21299895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73850254..73866426hg38UCSC Ensembl
Innerchr8:74762489..74778661hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3816173
hg1916173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087346
Samplessample308
Known GenesUBE2W
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116629
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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