A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209851



Internal ID22357866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64172546..64177228hg38UCSC Ensembl
chr20:62803899..62808581hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384683
hg194683
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5400n152
Supporting Variantsnssv14407853
SamplesNA19240
Known GenesMYT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209851
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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