A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1648n152



Internal ID22817351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134046061..134046152hg38UCSC Ensembl
chr11:133915956..133916047hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3528583, nsv3288450
SamplesNA19238, NA19240, HG00513
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1648n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer