A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541674



Internal ID316249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30240979..30252940hg38UCSC Ensembl
chr21:31613297..31625258hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3811962
hg1911962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541674
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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