A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521221



Internal ID297518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14884756..14885081hg38UCSC Ensembl
chr21:16257077..16257402hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521221
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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