nsv1197588 - (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:187,786
- Data Source:Published variants curated by OMIM and reviewed by NCBI staff
- Description:Approximately 190-kb microdeletion in FOXP1 spanning exons 7-13 of NG_028243.1 plus flanking genomic sequences. 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):Le Fevre et al. 2013
- Replacement Description: Replaced nstd51 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Replacement Variant: nsv3881933
This variant has been obsoleted and is no longer valid.