Human Genome Issue HG-185

Summary:

GeneID: 83538 (TTC25), missing in assembly

Description:

Possible assembly error or missing sequence affecting TTC25 (GeneID:83538)

Status:

Resolved (GRC Resolved by Electronic Means)

Type:

Clone Problem

Last updated:

2014-10-01

Affects version:

NCBI36

Fix version:

GRCh37.p3, GRCh38

Resolution:

This patch corrects a deletion found in GRCh37 chromosome NC_000017.10, in component AC091172.11, affecting TTC25 (GeneID:83538).

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 a deletion found in GRCh37 chromosome NC_000017.10, in component AC091172.11, affecting TTC25 (GeneID:83538).

Locations and genomic context

• GRCh38.p14 chr17:41,804,738-41,835,311 (View region: Ensembl | NCBI | UCSC)
• GRCh37.p13 chr17:39,960,990-40,117,363 (View region: Ensembl | NCBI | UCSC)
• GRCh37.p13 chr17|NW_003571052.1:91,380-121,953