A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093545



Internal ID20660585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119828201..119831200hg38UCSC Ensembl
chr3:119547048..119550047hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368378
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093545
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