A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992042



Internal ID21901385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141990913..141991611hg38UCSC Ensembl
chr3:141709755..141710453hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553817
Samples
Known GenesTFDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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