A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434421



Internal ID213096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180784692..180936709hg38UCSC Ensembl
chr3:180502480..180654497hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38152018
hg19152018
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944665
Samples
Known GenesFXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434421
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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