A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3116n152



Internal ID22818819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2863418..2869540hg38UCSC Ensembl
chr16:2913419..2919541hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386123
hg196123
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3197482, nsv3208174, nsv3209922
SamplesNA19240, HG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv3116n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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