A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209359



Internal ID20776399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49398077..49478018hg38UCSC Ensembl
chr3:49435510..49515451hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3879942
hg1979942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367330
Supporting Variants
Samples
Known GenesAMT, DAG1, NICN1, RHOA, TCTA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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