A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040302



Internal ID20607342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22445240..22447072hg38UCSC Ensembl
chr18:20025203..20027035hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381833
hg191833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533435
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00538


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