A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14407853



Internal ID22318480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64172546..64177228hg38UCSC Ensembl
chr20:62803899..62808581hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384683
hg194683
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209851
Supporting Variants
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)nssv14407853
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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