A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120853



Internal ID21466888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35483208..35483208hg38UCSC Ensembl
chr22:35879201..35879201hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669810
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120853
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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