A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121067



Internal ID21460745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47565740..47565740hg38UCSC Ensembl
chr22:47961489..47961489hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671102
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121067
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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