nsv915617 - (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:3
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:258,196
- 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: nsv3895505
- ClinVar: SCV000178701
- HP: 0000050
- HP: 0000369
- HP: 0000377
- HP: 0000534
- HP: 0000664
- HP: 0000707
- HP: 0000717
- HP: 0000739
- HP: 0000750
- HP: 0001263
- HP: 0001622
- HP: 0002099
- HP: 0002194
- HP: 0004279
- HP: 0004322
- HP: 0004324
- HP: 0006942
- HP: 0008760
- HP: 0009778
- HP: 0010554
- HP: 0010720
- HP: 0010862
- dbVar: nssv15139078
- dbVar: nsv4355848
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.