Variation class
CNV(SO:0001019)
Allele type(s)
deletion(SO:0000159)
Source
dbVar - NCBI database of human genomic structural variation
Study
nstd102 - Structural Variants with clinical assertions, submitted to ClinVar by external labs.
Alias
Clinical significance 
Location
Chromosome 16:29460515-30346868 (forward strand) | View in location tab
Inner coordinates: 16:29606852-30199854
Genomic size
886,354 bp
About this structural variant
This structural variant overlaps 362 transcripts, is associated with 1 phenotype and is supported by 1 piece of evidence.