A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5411473



Internal ID190780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79880208..79880242hg38UCSC Ensembl
chr9:82495123..82495157hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5411473
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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