A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507354



Internal ID284075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68204175..68211713hg38UCSC Ensembl
chr14:68670892..68678430hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg387539
hg197539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697777
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507354
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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