A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624586



Internal ID21816633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87365010..87365010hg38UCSC Ensembl
chr16:87398616..87398616hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093610
Supporting Variants
Samples
Known GenesFBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624586
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