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Human Genome Issue HG-1817

Summary:
Chromosome 13 assembly gap (FO538767.4 - FO624990.1)
Description:
Assembly gap between FO538767.4 (ABC8-41207300F1) and FO624990.1 (ABC8-43014700C16) in GRCh38. FO624990.1, a chimeric clone, was replaced by FP565796.3 in GRCh38.p1 (see HG-2216).
Status:
Resolved (GRC Resolved by Electronic Means)
Type:
Gap
Last updated:
2019-01-15
Affects version:
GRCh37
Fix version:
GRCh39, GRCh38.p13
Resolution:
CHM1 contig LJII02000026.1 closes the assembly gap between FO538767.4 and FP565796.3.

Patches and alternate loci

No patches or alts are associated with HG-1817.

Locations and genomic context

Select a placement below to display it in the Sequence Viewer.
  • GRCh38.p12 chr13:86,200,738-86,285,357 (View region: Ensembl | NCBI | UCSC)