Human Genome Issue HG-2373
- Summary:
- GeneID: 100508631 (LOC100508631), poor quality (includes component misassembly)
- Description:
- NC_000004.12 component AL136537.4 has a 12nt deletion relative to available human transcripts and orthologous regions in several other organisms.
- Status:
-
Resolved
(GRC Resolved- No Change)
- Type:
- Variation
- Last updated:
- 2021-06-10
- Affects version:
- GRCh38
- Fix version:
-
GRCh39
- Resolution:
- This 12nt deletion allele has support in the RP11 wgs illumina reads, HG03807 (GCA_003601015.1), and HG01352 (GCA_002209525.1) wgs assemblies. This variation does not meet the GRC criteria for reference update or alternate locus creation.
Patches and alternate loci
No patches or alts are associated with HG-2373.
Locations and genomic context
Select a placement below to display it in the Sequence Viewer.
