A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080741



Internal ID21437027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89325087..89325270hg38UCSC Ensembl
chr15:89868318..89868501hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588393
Supporting Variants
SamplesHG00731
Known GenesPOLG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080741
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer