A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089473



Internal ID21998706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89788220..89788220hg38UCSC Ensembl
chr14:90254564..90254564hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089473
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