A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564009



Internal ID336933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63471626..63659036hg38UCSC Ensembl
chr14:63938344..64125754hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38187411
hg19187411
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698131
Samples
Known GenesPPP2R5E, WDR89
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564009
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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