A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410630



Internal ID189945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109149979..109149979hg38UCSC Ensembl
chr9:111912259..111912259hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026698
Samples
Known GenesFRRS1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410630
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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