A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665816



Internal ID21614122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43153014..43153014hg38UCSC Ensembl
chr22:43549020..43549020hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120058
SamplesNA19238
Known GenesTSPO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665816
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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