A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192270



Internal ID22342880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43696684..43697189hg38UCSC Ensembl
chr20:42325324..42325829hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5275n152
Supporting Variantsnssv14449474
SamplesHG00733
Known GenesMYBL2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192270
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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