A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406902



Internal ID186239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137404417..137404468hg38UCSC Ensembl
chr8:138416660..138416711hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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