A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197779



Internal ID20764819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3560333..3569560hg38UCSC Ensembl
chr19:3560331..3569558hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389228
hg199228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197779
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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