A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089171



Internal ID21433223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109560819..109560819hg38UCSC Ensembl
chr13:110213166..110213166hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654357
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089171
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