A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191483



Internal ID22342183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22452204..22453093hg38UCSC Ensembl
chr18:20032167..20033056hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3785n152
Supporting Variantsnssv14446080
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)nsv3191483
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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