A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198856



Internal ID20765896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44909657..44924987hg38UCSC Ensembl
chr19:45412914..45428244hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3815331
hg1915331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528622
Supporting Variants
Samples
Known GenesAPOC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198856
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