A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107686



Internal ID21293260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:128808971..128813944hg38UCSC Ensembl
Innerchr4:129730126..129735099hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg384974
hg194974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115575
Supporting Variants
Samplessample98
Known GenesJADE1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107686
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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