A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210421



Internal ID20777461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23028267..23065576hg38UCSC Ensembl
chr3:23069758..23107067hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3837310
hg1937310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210421
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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