A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511518



Internal ID288096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113267438..113269454hg38UCSC Ensembl
chr13:113921752..113923768hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382017
hg192017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511518
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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