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Human Genome Issue HG-1169

Summary:
NOVEL patch created to capture sequence from AC208500.2 not represented in reference chromosome
Description:
NOVEL patch GL383552.1 created to capture sequence from AC208500.2 not represented in reference chromosome
Status:
Resolved (GRC Resolved by Electronic Means)
Type:
Variation
Last updated:
2014-10-01
Affects version:
GRCh37
Fix version:
GRCh37.p2, GRCh38
Resolution:
AC208500.2, which represents a sequence variant to GRCh37 by containing 7052bp more than component AC068305.30, has been uploaded to the Chr. 12 Alt-Ref-Loci TPF.

Patches and alternate loci

Scaffold type:
ALT in GRCh37
Comment:
In this scaffold, AC208500.2 represents a sequence variant containing 7052 bp that does not align to GRCh37 NC_000012.11 component AC068305.30.
Revision history of patches and alts for HG-1169
Assembly Scaffold type Contig name GenBank accession RefSeq accession Region
GRCh37.p2 NOVEL HSCHR12_2_CTG2_1 GL383552.1 NW_003315941.1 REGION23
GRCh38 ALT HSCHR12_2_CTG2_1 GL383552.1 NW_003315941.1 REGION23

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)