A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767391



Internal ID20543251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43743453..43743453hg38UCSC Ensembl
chr21:45163334..45163334hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283729
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767391
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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