A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209741



Internal ID22357771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68676819..68677008hg38UCSC Ensembl
chr18:66344056..66344245hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14447008
SamplesHG00733
Known GenesTMX3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209741
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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