A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016580



Internal ID20583620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20830704..20834134hg38UCSC Ensembl
chr14:21298863..21302293hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383431
hg193431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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