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 14:94833040-94854940 (forward strand) | View in location tab
Inner coordinates: 14:94843083-94854940
Genomic size
21,901 bp
About this structural variant
This structural variant overlaps 17 transcripts, is associated with 1 phenotype and is supported by 1 piece of evidence.