A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874084



Internal ID22649034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50370308..50371661hg38UCSC Ensembl
chr22:50808737..50810090hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg381354
hg191354
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484291
Samples
Known GenesPPP6R2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874084
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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