nsv497823 - (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:40
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:81,752
- Description: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: nsv3920442
- ClinVar: SCV000174323
- HP: 0000175
- HP: 0000204
- HP: 0000508
- HP: 0000707
- HP: 0000708
- HP: 0000717
- HP: 0000750
- HP: 0000953
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001263
- HP: 0001275
- HP: 0001510
- HP: 0001629
- HP: 0001631
- HP: 0001638
- HP: 0002487
- HP: 0007030
- dbVar: nssv15137779
- dbVar: nsv4356381
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.