A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203489



Internal ID22352491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55904141..55904499hg38UCSC Ensembl
chr18:53571372..53571730hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14419801
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203489
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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