A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580384



Internal ID21528874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120582738..120582804hg38UCSC Ensembl
chr5:119918433..119918499hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132267
SamplesHG03486
Known GenesPRR16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580384
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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