A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190774



Internal ID22341589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43696981..43697485hg38UCSC Ensembl
chr20:42325621..42326125hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14395536
SamplesNA19240
Known GenesMYBL2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190774
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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