A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433285



Internal ID212008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49106169..49106185hg38UCSC Ensembl
chr15:49398366..49398382hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433285
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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