A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1393n152



Internal ID22817096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56703270..56714334hg38UCSC Ensembl
chr11:56470746..56481810hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811065
hg1911065
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3200857, nsv3191620
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1393n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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