A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191131



Internal ID22341881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50768439..50771238hg38UCSC Ensembl
chr20:49384976..49387775hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14408887
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191131
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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