A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113725



Internal ID21296991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186448072..186452242hg38UCSC Ensembl
Innerchr3:186165861..186170031hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg384171
hg194171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108016
Samplessample321
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113725
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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