A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113891



Internal ID20680931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18854588..18854977hg38UCSC Ensembl
chr4:18856211..18856600hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00286


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