A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204691



Internal ID22353500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22452200..22453041hg38UCSC Ensembl
chr18:20032163..20033004hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3785n152
Supporting Variantsnssv14392968
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)nsv3204691
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer