A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931543



Internal ID21773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761621..35761671hg38UCSC Ensembl
chr3:35803113..35803163hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542620
Supporting Variants
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931543
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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