A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053599



Internal ID21962832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33071424..33089385hg38UCSC Ensembl
chr21:34443730..34461691hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3817962
hg1917962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649450
Samples
Known GenesOLIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053599
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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