A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666751



Internal ID21615058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24757659..24757659hg38UCSC Ensembl
chr22:25153626..25153626hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124000
SamplesNA24385
Known GenesPIWIL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666751
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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