A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731783



Internal ID20507704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133603657..133605403hg38UCSC Ensembl
chr3:133322501..133324247hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381747
hg191747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290420
Samples
Known GenesTOPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731783
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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