A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1626n152



Internal ID22817329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128868550..128868692hg38UCSC Ensembl
chr11:128738445..128738587hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3218007, nsv3220270
SamplesHG00512, HG00514
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)dgv1626n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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