A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419760



Internal ID198884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32689307..32689358hg38UCSC Ensembl
chr14:33158513..33158564hg19UCSC Ensembl
Cytoband14q12
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 Variantsnssv17693614
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419760
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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