HG-1380 - Human Genome Issues - Genome Reference Consortium

Trang chủ » Hg 1380 » HG-1380 - Human Genome Issues - Genome Reference Consortium

Có thể bạn quan tâm

GRC logoGenome Reference Consortium Skip navigation and go to main content
  • GRC Home
  • Data
    • Human Overview
    • Human Genome Issues
    • Human Assembly Data
  • Help
  • Report an Issue
  • Contact Us
  • Credits
  • Curators Only
Human Genome Issue HG-1380 Summary:There is gap between BX537339.3 and the centromere Description:There is gap between BX537339.3 and the centromere Status: Resolved (GRC Resolved by Electronic Means) Type: Gap Last updated:2019-11-05 Affects version: GRCh37 Fix version: GRCh39 Resolution: BX537339.3 has ~42kb of centromeric repeat on its end. The type-3 gap between BX537339.3 and the centromere has now been removed.

Patches and alternate loci

No patches or alts are associated with HG-1380.

Locations and genomic context

Select a placement below to display it in the Sequence Viewer.
  • GRCh38.p14 chrX:62,462,543-62,542,518 (View region: Ensembl | NCBI | UCSC)
  • GRCh37.p13 chrX:61,682,013-61,761,988 (View region: Ensembl | NCBI | UCSC)
  • FTP
  • NHGRI
  • Wellcome Sanger Institute
  • HHS
  • NIH
  • Accessibility
  • HHS Vulnerability Disclosure

Từ khóa » Hg 1380