A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3186n152



Internal ID22818889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24872948..24875758hg38UCSC Ensembl
chr16:24884269..24887079hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3202167, nsv3194558, nsv3196238
SamplesNA19240, HG00733, HG00514
Known GenesSLC5A11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv3186n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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