A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2967n152



Internal ID22818670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68133662..68136603hg38UCSC Ensembl
chr15:68426000..68428941hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382942
hg192942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3287415, nsv3529123, nsv3283922, nsv3286706
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesPIAS1
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)dgv2967n152
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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