A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492645



Internal ID269853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52939404..53170515hg38UCSC Ensembl
chr10:54699164..54930275hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38231112
hg19231112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492645
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