A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542491



Internal ID316904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110244351..110244376hg38UCSC Ensembl
chr9:113006631..113006656hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026799
Samples
Known GenesTXN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542491
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