A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376375



Internal ID22232418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89889767..89890179hg38UCSC Ensembl
chr15:90432999..90433411hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213232
Supporting Variants
SamplesHG00733
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376375
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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