A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4050n152



Internal ID22819753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:876664..880888hg38UCSC Ensembl
chr19:876664..880888hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384225
hg194225
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3195443, nsv3206337
SamplesNA19240, HG00733
Known GenesMED16
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv4050n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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