A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115185



Internal ID21298451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178777482..178792943hg38UCSC Ensembl
Innerchr5:178204483..178219944hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3815462
hg1915462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108881, nssv14109419
Samplessample340, sample181
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115185
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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