A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601546



Internal ID21793593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24003963..24049241hg38UCSC Ensembl
chr14:24473172..24518450hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3845279
hg1945279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026298
Supporting Variants
Samples
Known GenesDHRS4L1, DHRS4L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601546
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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