A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868449



Internal ID22643385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50768254..50770868hg38UCSC Ensembl
chr22:51206682..51209296hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg382615
hg192615
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484869
Samples
Known GenesRABL2B, RPL23AP82
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868449
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