A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198866



Internal ID22348537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63546516..63546582hg38UCSC Ensembl
chr20:62177869..62177935hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14395093
SamplesNA19240
Known GenesSRMS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198866
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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