A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193459



Internal ID22343902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18339158..18340758hg38UCSC Ensembl
chrUn_gl000212:167910..169510hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443669
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193459
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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