A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886508



Internal ID22661496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50754947..50766499hg38UCSC Ensembl
chr22:51193375..51204927hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3811553
hg1911553
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484863
Samples
Known GenesRPL23AP82
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886508
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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