nsv995235 - (obsolete)
- Organism: Homo sapiens
- Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:10
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:23,877
- 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: nsv3920070
- ClinVar: SCV000182652
- ClinVar: SCV000182654
- HP: 0000365
- HP: 0000729
- HP: 0000750
- HP: 0000752
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001263
- HP: 0001508
- HP: 0001622
- HP: 0002180
- HP: 0002194
- HP: 0002240
- HP: 0002260
- HP: 0010862
- HP: 0100806
- dbVar: nssv15138628
- dbVar: nssv15139272
- dbVar: nsv4349935
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.