A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951468



Internal ID22726828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43922685..43922749hg38UCSC Ensembl
chr21:45342566..45342630hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389959
Samples
Known GenesAGPAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951468
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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