A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092947



Internal ID21483070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79516325..79516325hg38UCSC Ensembl
chr16:79550222..79550222hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382998
hg192998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661201
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092947
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