A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045746



Internal ID21955005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45268860..45268912hg38UCSC Ensembl
chr21:46688775..46688827hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639756
Samples
Known GenesPOFUT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045746
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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