A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731508



Internal ID155174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21046050..21046050hg38UCSC Ensembl
chr20:21026691..21026691hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731508
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.436458


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