CONTIG

The CONTIG line is used for only CON data.

The CONTIG line is used to describe the order of cited sequences and gaps with a format similar to Description of Location for features.

example
CONTIG      join(BZZZ01123456.1:1..1345,gap(1500),BZZZ01123457.1:1..1456,
            gap(unk100),complement(BZZZ01123458.1:1..1230))

join([location1],[location2], ... [location3])

－－ the indicated elements should be joined (placed end-to-end) to form one contiguous sequence

BZZZ01123456.1:1..1345

－－ the sequence cited from 1st to 1345th nucleotides of WGS entry, BZZZ0112346.

gap(1500)

－－ estimated length gap, replaced by 1500 "n"s

BZZZ01123457.1:1..1456

－－ the sequence cited from 1st to 1456th nucleotides of WGS entry, BZZZ0112347.

gap(unk100)

－－ unknown length gap, replaced by 100 "n"s

complement(BZZZ01123458.1:1..1230)

－－ complementary strand of the sequence cited from 1st to 1230th nucleotides of WGS entry, BZZZ0112348.