A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2968n152



Internal ID22818671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68257829..68257889hg38UCSC Ensembl
chr15:68550167..68550227hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3226501, nsv3222590
SamplesNA19238, HG00731, HG00732, HG00733, HG00514
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2968n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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