A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115020



Internal ID21298286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178137963..178143634hg38UCSC Ensembl
Innerchr3:177855751..177861422hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385672
hg195672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106429
Samplessample146
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115020
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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