A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420855



Internal ID199946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118176112..118176163hg38UCSC Ensembl
chr12:118613917..118613968hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684789
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420855
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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