A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726444



Internal ID150110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26966804..26966857hg38UCSC Ensembl
chr21:28339123..28339176hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531222
Supporting Variants
Samples
Known GenesADAMTS5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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