A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202092



Internal ID22351299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79684893..79684972hg38UCSC Ensembl
chr18:77444893..77444972hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14419994
SamplesHG00514
Known GenesCTDP1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202092
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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