A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420336



Internal ID199440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54562164..54562215hg38UCSC Ensembl
chr14:55028882..55028933hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420336
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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