A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406266



Internal ID185606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88484825..88484876hg38UCSC Ensembl
chr9:91099740..91099791hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406266
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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