A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380452



Internal ID22438322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86857780..86857846hg38UCSC Ensembl
chr15:87401011..87401077hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943883
Supporting Variants
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380452
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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