A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397280



Internal ID176687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157483378..157483429hg38UCSC Ensembl
chr2:158339890..158339941hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16921605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397280
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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