A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084489



Internal ID20651529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23943769..23948463hg38UCSC Ensembl
chr2:24166639..24171333hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg384695
hg194695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346048
Supporting Variants
Samples
Known GenesUBXN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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