A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849983



Internal ID22033626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40580272..40580272hg38UCSC Ensembl
chr20:39208912..39208912hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849983
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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