A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667809



Internal ID21616114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49775817..49775817hg38UCSC Ensembl
chr22:50169465..50169465hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124649
SamplesNA19239
Known GenesBRD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667809
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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