A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477438



Internal ID255020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109355153..109355254hg38UCSC Ensembl
chr9:112117433..112117534hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477438
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer