A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406447



Internal ID185787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170316619..170316670hg38UCSC Ensembl
chr3:170034407..170034458hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943420
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406447
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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