A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848291



Internal ID22031934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22619054..22619054hg38UCSC Ensembl
chr20:22599692..22599692hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251321
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848291
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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