Human (GRCh37.p13)
Variation class

mobile element insertion(SO:0001837)

Allele type(s)

mobile element insertion(SO:0001837)

Source

DGVa - Database of Genomic Variants Archive

Study

estd59 - 1000 Genomes Project Consortium - Pilot Project. PMID:20981092 [remapped from build NCBI36]

Alias

P2_MEI_44

Location

Chromosome 10:73193532-73193533 (forward strand) | View in location tab
Outer coordinates: 10:73193514-73193551
Inner coordinates: 10:73193550-73193515

About this structural variant

This structural variant overlaps 4 transcripts and is supported by 2 pieces of evidence.