A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4166n152



Internal ID22819869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17349123..17349226hg38UCSC Ensembl
chr19:17459932..17460035hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3228586, nsv3299272
SamplesHG00732, HG00733
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)dgv4166n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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