A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14403245



Internal ID22318469
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 StatusS
Merged Variantsnsv3210815
Supporting Variants
SamplesNA19240
Known GenesTFDP1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14403245
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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