A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886189



Internal ID22661175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47122366..47128065hg38UCSC Ensembl
chr22:47518262..47523901hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg385700
hg195640
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484221
Samples
Known GenesTBC1D22A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886189
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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