A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1309n152



Internal ID22817012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28430923..28431142hg38UCSC Ensembl
chr11:28452470..28452689hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285124, nsv3283215
SamplesHG00733, 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)dgv1309n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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