nsv1197586 - (obsolete)
- Organism: Homo sapiens
- Study:nstd51 (obsolete - User submitted curated variants)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:27,558
- Data Source:Published variants curated by OMIM and reviewed by NCBI staff
- Description:Duplication of exons 11-12 from cDNA of gene GLB1. PLEASE NOTE: The calls represented in this region now have equivalents in the study Clinical Structural Variants (nstd102). Please use the preferred nstd102 variant region accession for this variant; you can find it at top right under "Links to Other Resources" or in the mapping file provided here.
- Publication(s):Yoshida et al. 1991
- Replacement Description: Replaced nstd51 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Replacement Variant: nsv3874698
This variant has been obsoleted and is no longer valid.