A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033951



Internal ID21943294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73294525..73294848hg38UCSC Ensembl
chr14:73761233..73761556hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613289
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033951
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer