A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4362n152



Internal ID22820065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55159745..55159820hg38UCSC Ensembl
chr19:55671113..55671188hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3298714, nsv3535616
SamplesHG00732, HG00733
Known GenesDNAAF3
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)dgv4362n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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