A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562483



Internal ID335437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68441266..68831279hg38UCSC Ensembl
chr14:68907983..69297996hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38390014
hg19390014
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697792
Samples
Known GenesRAD51B, ZFP36L1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562483
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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