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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.
Revision history of patches and alts for HG-544
Assembly Scaffold type Contig name GenBank accession RefSeq accession Region
GRCh37.p2 FIX HG544_PATCH GL383543.1 NW_003315932.1 FAM23A_MRC1

Locations and genomic context

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  • (View region: Ensembl | NCBI | UCSC)
  • (View region: Ensembl | NCBI | UCSC)