A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2908n152



Internal ID22818611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43014865..43014962hg38UCSC Ensembl
chr15:43307063..43307160hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3221397, nsv3213595
SamplesHG00512, NA19238, NA19239, NA19240, HG00513, HG00514
Known GenesUBR1
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)dgv2908n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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