A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200198



Internal ID22349684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17659116..17659197hg38UCSC Ensembl
chr20:17639761..17639842hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14449365
SamplesHG00733
Known GenesRRBP1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200198
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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