A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598093



Internal ID21790137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58254340..58254340hg38UCSC Ensembl
chr14:58721058..58721058hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085735
Supporting Variants
Samples
Known GenesPSMA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598093
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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