A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726140



Internal ID149806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17743172..17747818hg38UCSC Ensembl
chr21:19115489..19120135hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384647
hg194647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726140
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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