A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626215



Internal ID21574520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142924341..142924341hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3886
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149924
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626215
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