A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2429n152



Internal ID22818132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109293353..109293788hg38UCSC Ensembl
chr13:109945701..109946136hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3223247, nsv3225316
SamplesHG00514
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)dgv2429n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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