A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510599



Internal ID287210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94641843..94647162hg38UCSC Ensembl
chr11:94375009..94380328hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385320
hg195320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510599
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