nsv915682 - (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:16
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:606,788
- 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: nsv3919143
- ClinVar: SCV000178769
- ClinVar: SCV000178771
- HP: 0000156
- HP: 0000202
- HP: 0000252
- HP: 0000271
- HP: 0000316
- HP: 0000319
- HP: 0000598
- HP: 0000750
- HP: 0000821
- HP: 0000855
- HP: 0001263
- HP: 0001363
- HP: 0001397
- HP: 0001508
- HP: 0001513
- HP: 0001622
- HP: 0001631
- HP: 0002014
- HP: 0002194
- HP: 0002607
- HP: 0002650
- HP: 0003468
- HP: 0004322
- HP: 0005616
- dbVar: nssv15135520
- dbVar: nssv15135833
- dbVar: nsv4355355
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.