Human (GRCh37.p13)
Variation class

translocation(SO:0000199)

Allele type(s)

interchromosomal translocation(SO:0002060)

Source

DGVa - Database of Genomic Variants Archive

Study

estd210 - Blake 2014 "Analysis of Structural Variation in a patient with neurodevelopmental disease and balanced chromosomal abnormalities. We have used mate-pair sequencing to investigate the structural variation and possible genetic cause of disorder a high resolution."

Location

This feature maps to 2 genomic locations

Selected location
About this structural variant

This structural variant overlaps 3 transcripts and is supported by 1 piece of evidence.