A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507559



Internal ID284274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59434497..59441841hg38UCSC Ensembl
chr13:60008631..60015975hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg387345
hg197345
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507559
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer