A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541190



Internal ID21865545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62599779..62599779hg38UCSC Ensembl
chr3:62585454..62585454hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063458
Supporting Variants
Samples
Known GenesCADPS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541190
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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