A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602848



Internal ID21551508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38807254..38807429hg38UCSC Ensembl
chr22:39203259..39203434hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124309
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602848
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