A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420369



Internal ID199473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25968081..25968132hg38UCSC Ensembl
chr18:23548045..23548096hg19UCSC Ensembl
Cytoband18q11.2
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 Variantsnssv17716773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420369
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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