A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115550



Internal ID21485798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11102394..11102394hg38UCSC Ensembl
chr20:11083042..11083042hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666425
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115550
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