Variation class
CNV(SO:0001019)
Allele type(s)
deletion(SO:0000159)
Source
DGVa - Database of Genomic Variants Archive
Study
nstd108 - e 2015 "A 79-bp deletion detected during whole genome sequencing. Related single-nucleotide variation can be found in [dbSNP|http://www.ncbi.nlm.nih.gov/projects/SNP/snp_viewBatch.cgi?sbid"
Alias
OAR3-130010065-DEL
Location
Chromosome 3:130010066-130010144 (forward strand) | View in location tab
Genomic size
79 bp
About this structural variant
This structural variant is supported by 1 piece of evidence.
