A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1434n152



Internal ID22817137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68372261..68372391hg38UCSC Ensembl
chr11:68139729..68139859hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3229139, nsv3214605
SamplesHG00733
Known GenesLRP5
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)dgv1434n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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