A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191504



Internal ID20758544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17020266..17481020hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38460755
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191504
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.97753


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer