A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525696



Internal ID301846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22522875..22532000hg38UCSC Ensembl
chr18:20102838..20111963hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg389126
hg199126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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