nsv931145 - (obsolete)
- Organism: Homo sapiens
- Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:6
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:4,925,166
- 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: nsv3905431
- ClinVar: SCV000180645
- ClinVar: SCV000502923
- HP: 0000028
- HP: 0000347
- HP: 0000494
- HP: 0001250
- HP: 0001252
- HP: 0001307
- HP: 0001508
- HP: 0001622
- HP: 0001943
- HP: 0002098
- HP: 0002117
- HP: 0002194
- HP: 0002260
- HP: 0006905
- HP: 0011968
- dbVar: nssv15147508
- dbVar: nssv15149800
- dbVar: nsv3905431
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.