A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665302



Internal ID21613607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37227372..37227372hg38UCSC Ensembl
chr22:37623412..37623412hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136861
SamplesNA19238
Known GenesRAC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665302
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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