A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397060



Internal ID176470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91510812..91510812hg38UCSC Ensembl
chr9:94273094..94273094hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397060
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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