A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136771



Internal ID21502334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139780460..139780460hg38UCSC Ensembl
chr3:139499302..139499302hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606196
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136771
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