A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081726



Internal ID21479810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45577321..45577321hg38UCSC Ensembl
chr15:45869519..45869519hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652470
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081726
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