A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099213



Internal ID20666253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41271492..41271986hg38UCSC Ensembl
chr3:41312983..41313477hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366025
Supporting Variants
Samples
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099213
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