A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665732



Internal ID21614037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25792353..25792353hg38UCSC Ensembl
chr22:26188320..26188320hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128458
SamplesHG00512
Known GenesMYO18B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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