A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203344



Internal ID22352373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62343639..62343751hg38UCSC Ensembl
chr18:60010872..60010984hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456817
SamplesHG00733
Known GenesTNFRSF11A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203344
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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