A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198252



Internal ID20765292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49540406..49586977hg38UCSC Ensembl
chr19:50043663..50090234hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3846572
hg1946572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521022
Supporting Variants
Samples
Known GenesNOSIP, PRRG2, RCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198252
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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