FGviewer:

    We analyzed dbVar data (version of November 1st, 2019), which is the NCBI’s database of human genomic structural variation, and identified 40K FGs from 6M SV regions. Users can click interesting genomic studies gathered in dbVar and directly can go to the FGviewer analysis page for individual SV breakpoints of 40K FGs. Specifically, we found 1,037 FGs from the SVs detected from the Genome Aggregation Database (genomAD v2.1) of 15K population WGS data. Furthermore, one study (dbVar study ID: nstd33) in dbVar identified a recurrent 15q24 microdeletion from multiple individuals with mental retardation. From the SVs in 15q24 location, detected in this study, we have found one novel FG, CELF6-TMEM266.

Num

Date on dbVar

Publication

Study ID

Organism

# variant regions

# variant calls

# FGs

# FGBPs

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