nsv529243 - (obsolete)
- Organism: Homo sapiens
- Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:23
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:597,786
- Description:See descriptions for individual calls in download files. 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):Miller et al. 2010
- Replacement Description: Replaced nstd37 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Replacement Variant: nsv3910128
- ClinVar: SCV000175256
- ClinVar: SCV000175258
- ClinVar: SCV000175259
- ClinVar: SCV000175260
- HP: 0000256
- HP: 0000365
- HP: 0000717
- HP: 0000750
- HP: 0001249
- HP: 0001263
- HP: 0001337
- HP: 0001508
- HP: 0001513
- HP: 0001638
- HP: 0001651
- HP: 0002937
- HP: 0006510
- HP: 0007018
- dbVar: nssv15132259
- dbVar: nssv15132516
- dbVar: nsv3922004
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.