nsv1067861 - (obsolete)
- Organism: Homo sapiens
- Study:nstd51 (obsolete - User submitted curated variants)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:36,900
- Data Source:Published variants curated by OMIM and reviewed by NCBI staff
- Description:Deletion beginning in the CDS in exon 9 and extending in exon 23, resulting in the deletion of exons 3-23 from RB1CC1. 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):Chano et al. 2002
- Replacement Description: Replaced nstd51 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Replacement Variant: nsv3878401
This variant has been obsoleted and is no longer valid.