nsv491589 - (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:44
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:1,765,645
- 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: nsv3915267
- ClinVar: SCV000172965
- ClinVar: SCV000172966
- HP: 0000204
- HP: 0000478
- HP: 0000518
- HP: 0000707
- HP: 0000717
- HP: 0000729
- HP: 0000752
- HP: 0001159
- HP: 0001252
- HP: 0001263
- HP: 0001508
- HP: 0002086
- HP: 0002117
- HP: 0002370
- HP: 0002384
- HP: 0002475
- HP: 0010442
- dbVar: nssv15146162
- dbVar: nssv15146308
- dbVar: nsv4358672
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.