A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549306



Internal ID21873661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16537885..16537885hg38UCSC Ensembl
chr3:16579392..16579392hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051210
Supporting Variants
Samples
Known GenesLINC00690
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549306
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