A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3287098



Internal ID22385499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89325035..89325233hg38UCSC Ensembl
chr15:89868266..89868464hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3019n152
Supporting Variantsnssv14430909, nssv14467544
SamplesHG00733, HG00514
Known GenesPOLG
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3287098
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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