A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732521



Internal ID20508445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142021369..142022534hg38UCSC Ensembl
chr3:141740211..141741376hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258938
Samples
Known GenesTFDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732521
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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