A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152642



Internal ID21454257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23048162..23048162hg38UCSC Ensembl
chr8:22905675..22905675hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381080
hg191080
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633217
Supporting Variants
SamplesHG02011
Known GenesTNFRSF10B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152642
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