A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207920



Internal ID20774960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119970906..119975465hg38UCSC Ensembl
chr3:119689753..119694312hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg384560
hg194560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362747
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207920
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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