A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991653



Internal ID21900996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146528153..146528298hg38UCSC Ensembl
chr3:146245940..146246085hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556574
Samples
Known GenesPLSCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991653
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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