A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859222



Internal ID22634157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122845224..122847615hg38UCSC Ensembl
chr9:125607503..125609894hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382392
hg192392
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859222
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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