A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2500n152



Internal ID22818203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113625011..113625160hg38UCSC Ensembl
chr13:114279326..114279475hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3210815, nsv3229754
SamplesNA19240
Known GenesTFDP1
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)dgv2500n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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