A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761654



Internal ID20537514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5169353..5169353hg38UCSC Ensembl
chr3:5211038..5211038hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382536
hg192536
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260591
Samples
Known GenesARL8B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761654
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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