A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184928



Internal ID20751968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55155699..55223378hg38UCSC Ensembl
chr14:55622417..55690096hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3867680
hg1967680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491221
Supporting Variants
Samples
Known GenesDLGAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184928
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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