A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037983



Internal ID21947326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67921851..67923965hg38UCSC Ensembl
chr14:68388568..68390682hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606942
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037983
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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