A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210453



Internal ID20777493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25663701..25665300hg38UCSC Ensembl
chr3:25705192..25706791hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357211
Supporting Variants
Samples
Known GenesMIR4442, TOP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210453
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00011


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