A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725989



Internal ID149655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43307338..43308054hg38UCSC Ensembl
chr20:41935978..41936694hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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