A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091673



Internal ID21491891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113279047..113279047hg38UCSC Ensembl
chr13:113933362..113933362hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663128
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091673
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