A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199632



Internal ID20766672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5548901..5552800hg38UCSC Ensembl
chr19:5548912..5552811hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199632
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