A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732216



Internal ID155882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36776298..36776349hg38UCSC Ensembl
chr20:35404701..35404752hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427332
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732216
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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