A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121241



Internal ID21504812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39673959..39673959hg38UCSC Ensembl
chr3:39715450..39715450hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620300
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121241
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