A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510868



Internal ID287476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56682074..56759108hg38UCSC Ensembl
chr13:57256208..57333242hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3877035
hg1977035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510868
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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