A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380773



Internal ID22324089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66146781..66148011hg38UCSC Ensembl
chr13:66720913..66722143hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208473
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)nssv14380773
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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