A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040498



Internal ID21949841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43975202..43975255hg38UCSC Ensembl
chr21:45395083..45395136hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648387
Samples
Known GenesAGPAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040498
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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