A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084364



Internal ID21435386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88897514..88897514hg38UCSC Ensembl
chr15:89440745..89440745hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660417
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084364
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