A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021722



Internal ID21931065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60128739..60130633hg38UCSC Ensembl
chr14:60595457..60597351hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381895
hg191895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614465
Samples
Known GenesPCNXL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021722
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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