A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494094



Internal ID271252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110042000..110052979hg38UCSC Ensembl
chr13:110694347..110705326hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3810980
hg1910980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494094
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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