A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023085



Internal ID20590126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98327490..98327972hg38UCSC Ensembl
chr14:98793827..98794309hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496519
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00063


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