A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208653



Internal ID20775695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41872588..42175248hg38UCSC Ensembl
chr3:41914080..42216740hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38302661
hg19302661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360144
Supporting Variants
Samples
Known GenesTRAK1, ULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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