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Human Genome Issue HG-1153

Summary:
NOVEL patch created to capture sequence from AC225889.3 not represented in reference chromosome
Description:
NOVEL patch GL383529.1 created to capture sequence from AC225889.3 not represented in reference chromosome
Status:
Resolved (GRC Resolved by Electronic Means)
Type:
Variation
Last updated:
2015-07-23
Affects version:
GRCh37
Fix version:
GRCh37.p2, GRCh38
Resolution:
AC225889.3 is suspected to be a chimeric clone and will not be included as an ALT_LOCI in GRCh38.

Patches and alternate loci

Scaffold type:
NOVEL patch to GRCh37
Comment:
In this scaffold, AC225889.3 represents a sequence variant containing approximately 21kb that does not align to GRCh37 NC_000004.11 component AC092663.2.
Revision history of patches and alts for HG-1153
Assembly Scaffold type Contig name GenBank accession RefSeq accession Region
GRCh37.p2 NOVEL HSCHR4_2_CTG9 GL383529.1 NW_003315916.1 LPHN3

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)