A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547651



Internal ID21872006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17522592..17531467hg38UCSC Ensembl
chr3:17564084..17572959hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388876
hg198876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992142
Supporting Variants
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547651
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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