A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197039



Internal ID20764079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78830033..78848725hg38UCSC Ensembl
chr16:78863930..78882622hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818693
hg1918693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502119
Supporting Variants
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197039
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