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Human Genome Issue HG-1699

Summary:
Assembly component AC104995.4 contains a possible erroneous inversion
Description:
Assembly component AC104995.4 contains a possible erroneous inversion.
Status:
Resolved (GRC Resolved by Experimental Method)
Type:
Clone Problem
Last updated:
2015-07-23
Fix version:
GRCh37.p13, GRCh38
Resolution:
Assembly component AC104995.4 has been replaced with fosmids that contain the correct orientation of this inverted piece of sequence.

Patches and alternate loci

Scaffold type:
FIX patch to GRCh37
Comment:
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 corrects an erroneous inversion found in component AC104995.4 in GRCh37 chromosome NC_000008.10.
Revision history of patches and alts for HG-1699
Assembly Scaffold type Contig name GenBank accession RefSeq accession Region
GRCh37.p13 FIX HG1699_PATCH KE332500.1 NW_004775431.1 REGION102

Locations and genomic context

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