A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115019



Internal ID21298285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:30501184..30509649hg38UCSC Ensembl
Innerchr5:30501291..30509756hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg388466
hg198466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108942
Samplessample196
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115019
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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