A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451465



Internal ID229647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24014678..24014832hg38UCSC Ensembl
chr3:24056169..24056323hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451465
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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