A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547981



Internal ID21872336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48170278..48170677hg38UCSC Ensembl
chr3:48211768..48212167hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993486
Supporting Variants
Samples
Known GenesCDC25A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547981
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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