A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165372



Internal ID20732413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19696258..19728958hg38UCSC Ensembl
chr8:19553769..19586469hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3832701
hg1932701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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