A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109494



Internal ID20676534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14629846..14630683hg38UCSC Ensembl
chr4:14631470..14632307hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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