A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094282



Internal ID20661322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141058119..141059835hg38UCSC Ensembl
chr3:140776961..140778677hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381717
hg191717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357545
Supporting Variants
Samples
Known GenesSPSB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00153


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