A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2436n152



Internal ID22818139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109665951..109666016hg38UCSC Ensembl
chr13:110318298..110318363hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3219886, nsv3284554
SamplesNA19238, NA19240, HG00733
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)dgv2436n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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