A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030647



Internal ID21939990
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 StatusM
Merged Variants
Supporting Variantsnssv17614892
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030647
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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