A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5255n152



Internal ID22820958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35906443..35906542hg38UCSC Ensembl
chr20:34494365..34494464hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3218386, nsv3292670
SamplesHG00732, HG00733
Known GenesPHF20
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)dgv5255n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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