Human Genome Issue HG-544
- Chr.10 Gap Problem
- There is a gap in the assembly between components BX255924.4 and AL928729.2
- Resolved (GRC Resolved by Experimental Method)
- Last updated:
- Fix version:
- GRCh37.p2, GRCh38
- Artificial gap caused by artificial duplication of flanking regions. Confirmed by FibreFISH and Optical Map data. Components AL928580, BX255924 and AL928729 removed from the reference and gap closed.
Patches and alternate loci
- Scaffold type:
- FIX patch to GRCh37
- This sequence will be incorporated into the reference assembly in the next major assembly release. At that time, the accession number for this patch will be made secondary to the reference chromosome accession. This patch closes the gap in GRCh37 NC_000010.10 at nt 17,974,676-18,024,675 by the removal of components AL928580.4, BX255924.4 and AL928729.2.
|Assembly||Scaffold type||Contig name||GenBank accession||RefSeq accession||Region|