A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742936



Internal ID20518922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121607370..121607470hg38UCSC Ensembl
chr3:121326217..121326317hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275205
Samples
Known GenesFBXO40
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742936
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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