A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489273



Internal ID266562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90836021..90923610hg38UCSC Ensembl
chr9:93598303..93685892hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3887590
hg1987590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024026
Samples
Known GenesSYK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489273
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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