A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887099



Internal ID22662091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35769898..35774469hg38UCSC Ensembl
chr22:36165945..36170516hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384572
hg194572
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482906
Samples
Known GenesRBFOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887099
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