A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614892



Internal ID21806939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68356153..68356704hg38UCSC Ensembl
chr14:68822870..68823421hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030647
Supporting Variants
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614892
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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