nsv916206 - (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:9
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:94,668,398
- 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: nsv3921223
- ClinVar: SCV000179328
- HP: 0000175
- HP: 0000204
- HP: 0000218
- HP: 0000252
- HP: 0000322
- HP: 0000494
- HP: 0000750
- HP: 0000879
- HP: 0000954
- HP: 0001249
- HP: 0001263
- HP: 0001290
- HP: 0001508
- HP: 0001539
- HP: 0001561
- HP: 0001635
- HP: 0001636
- HP: 0001999
- HP: 0002194
- HP: 0002260
- HP: 0008551
- HP: 0010442
- HP: 0010862
- HP: 0011951
- HP: 0012304
- dbVar: nssv15161365
- dbVar: nsv4354590
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.