A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379638



Internal ID22195151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86296413..86296476hg38UCSC Ensembl
chr15:86839644..86839707hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226033
Supporting Variants
SamplesHG00731
Known GenesAGBL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379638
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