A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665430



Internal ID21613735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36165240..36165240hg38UCSC Ensembl
chr22:36561288..36561288hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132549
SamplesNA19239
Known GenesAPOL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665430
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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