A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183024



Internal ID20750064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78067370..78161608hg38UCSC Ensembl
chr16:78101267..78195505hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3894239
hg1994239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496087
Supporting Variants
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183024
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