A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082890



Internal ID21992123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63815212..63815212hg38UCSC Ensembl
chr14:64281930..64281930hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082890
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