A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201138



Internal ID22350487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62343511..62343596hg38UCSC Ensembl
chr18:60010744..60010829hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14447473
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)nsv3201138
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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