A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418902



Internal ID198056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101766331..101766367hg38UCSC Ensembl
chr14:102232668..102232704hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697380
Samples
Known GenesPPP2R5C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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