A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482256



Internal ID259714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84201688..84203062hg38UCSC Ensembl
chr9:86816603..86817977hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381375
hg191375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482256
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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