Variation class
insertion(SO:0000667)
Allele type(s)
insertion(SO:0000667)
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 17:61565892 (forward strand) | View in location tab
About this structural variant
This structural variant overlaps 13 transcripts, is associated with 11 phenotypes and is supported by 7 pieces of evidence.