A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438066



Internal ID216637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133908315..133925460hg38UCSC Ensembl
chr3:133627159..133644304hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3817146
hg1917146
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937790
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438066
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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