A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540537



Internal ID315289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32959298..32966406hg38UCSC Ensembl
chr21:34331606..34338714hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg387109
hg197109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540537
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer