A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516353



Internal ID292812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25782786..25786983hg38UCSC Ensembl
chr21:27155097..27159294hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384198
hg194198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516353
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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