A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410540



Internal ID189855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107299652..107299703hg38UCSC Ensembl
chr9:110061933..110061984hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028244
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410540
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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