A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084462



Internal ID21993695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67973869..67973869hg38UCSC Ensembl
chr14:68440586..68440586hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601570
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084462
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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