A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107547



Internal ID21291589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177210435..178187882hg38UCSC Ensembl
Innerchr4:178131589..179109036hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38977448
hg19977448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113325
Supporting Variants
Samplessample77
Known GenesAGA, LINC01098, LINC01099, NEIL3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107547
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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