A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4081n152



Internal ID22819784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3173259..3175787hg38UCSC Ensembl
chr19:3173257..3175785hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382529
hg192529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3291605, nsv3220092
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00513, 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)dgv4081n152
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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