A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992679



Internal ID21902022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188356896..188376315hg38UCSC Ensembl
chr3:188074684..188094103hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3819420
hg1919420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552289
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992679
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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