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Human Genome Issue HG-1692

Summary:
RPCI-11 components on the Chromosome 15 Unlocalized TPF align to the Prader-Willi region and either represent an alternate haplotype or missing sequence in the Reference.
Description:
Three RPCI-11 library clones which align to the Prader-Willi region of Chromosome 15 need localized.
Status:
Resolved (GRC Resolved by Electronic Means)
Type:
Localization Problem
Last updated:
2019-02-05
Experiment type:
Clone Sequencing
Affects version:
GRCh37.p12
Fix version:
GRCh39
Resolution:
This TPF has been removed from the Chr. 15 unlocalized TPF. With the addition of the CH17 clone pathway replacing the RP11 Prader-Willi region, this sequence is no long unique/unlocalized.

Patches and alternate loci

No patches or alts are associated with HG-1692.

Locations and genomic context

Select a placement below to display it in the Sequence Viewer.
  • (View region: Ensembl | NCBI | UCSC)
  • (View region: Ensembl | NCBI | UCSC)
  • (View region: Ensembl | NCBI | UCSC)