A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599797



Internal ID21548434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45037518..45037877hg38UCSC Ensembl
chr22:45433399..45433758hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136742
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599797
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