A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731674



Internal ID155340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24268804..24269641hg38UCSC Ensembl
chr20:24249440..24250277hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731674
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01624


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