A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210452



Internal ID20777492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25658101..25664200hg38UCSC Ensembl
chr3:25699592..25705691hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360880
Supporting Variants
Samples
Known GenesTOP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210452
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00087


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