A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193481



Internal ID22343924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64172573..64177466hg38UCSC Ensembl
chr20:62803926..62808819hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384894
hg194894
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5400n152
Supporting Variantsnssv14432727, nssv14432726
SamplesHG00514
Known GenesMYT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193481
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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