A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094384



Internal ID20661424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14317364..14331300hg38UCSC Ensembl
chr3:14358864..14372800hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3813937
hg1913937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357153
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094384
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