A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848296



Internal ID22031939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22965860..22965860hg38UCSC Ensembl
chr20:22946497..22946497hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251326
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848296
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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