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Human Genome Region DLGAP4

Assembly:
GRCh37.p12
Location:
chr20:34,883,261-34,994,224
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-144 Resolved There is a gap in build 36 between AL512784.6 and AL450465.12. nts 1-133 of NM_014902.3 are GC rich; BLAST with no filter indicates these align at 100% to AL512784.6 whereas the remainder of NM_014902.3 aligns to the components of NT_011362.9, of which AL450465.12 is the first one across the gap. The PCR product JN854134.1 was used to bridge the gap between FP565784.3 and FP565581.3.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH720448.1 NW_003871095.1 FIX 70,483 2 9,519
           

DLGAP4 -- chr20 (NC_000020.10):34,883,261-34,994,224