A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208655



Internal ID20775697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42013699..42140145hg38UCSC Ensembl
chr3:42055191..42181637hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38126447
hg19126447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368943
Supporting Variants
Samples
Known GenesTRAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208655
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