A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4158n152



Internal ID22819861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15651126..15651600hg38UCSC Ensembl
chr19:15761936..15762410hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3300918, nsv3533056
SamplesHG00512, HG00514
Known GenesCYP4F3
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)dgv4158n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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