Variation class
CNV(SO:0001019)
Allele type(s)
gain(SO:0001742)
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 2:1905043-2216475 (forward strand) | View in location tab
Genomic size
311,433 bp
About this structural variant
This structural variant overlaps 7 transcripts, is associated with 1 phenotype and is supported by 1 piece of evidence.