A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545470



Internal ID21869825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32753697..32753697hg38UCSC Ensembl
chr3:32795189..32795189hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg383133
hg193133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063814
Supporting Variants
Samples
Known GenesCNOT10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545470
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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