A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628593



Internal ID21820640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50785418..50785418hg38UCSC Ensembl
chr16:50819329..50819329hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090323
Supporting Variants
Samples
Known GenesCYLD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628593
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