A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059062



Internal ID21968295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44818387..44818491hg38UCSC Ensembl
chr21:46238302..46238406hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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