A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14403093



Internal ID22314172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111669490..111669613hg38UCSC Ensembl
chr13:112321837..112321960hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206312
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14403093
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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