Skip navigation and go to main content

Human Genome Region REGION82

Assembly:
GRCh37.p11
Location:
chr9:137,025,633-137,247,659
Cytogenetic location:

Loading ideogram...

Genome issues
Issue ID Status Description Resolution text
HG-1500 Resolved There is a gap in the assembly between components BX649601.2 and AL354796.21. This is a duplicate issue used for patch release of an extension from the left side into the gap. There is a gap in the assembly between components BX649601.2 and AL354796.21. This is a duplicate issue used for patch release of an extension from the left side into the gap.
HG-1501 Resolved There is a gap in the assembly between components BX649601.2 and AL354796.21. This is a duplicate issue used for patch release of an extension from the right side into the gap. There is a gap in the assembly between components BX649601.2 and AL354796.21. This is a duplicate issue used for patch release of an extension from the right side into the gap.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH806577.1 NW_004070867.1 FIX 22,394 0 6,833
JH806578.1 NW_004070868.1 FIX 169,437 1 12,972
           

REGION82 -- chr9 (NC_000009.11):137,025,633-137,247,659