nsv996099 - (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:18
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:80,120,014
- 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: nsv3907722
- ClinVar: SCV000183529
- ClinVar: SCV000586681
- HP: 0000041
- HP: 0000126
- HP: 0000237
- HP: 0000239
- HP: 0000347
- HP: 0000369
- HP: 0000478
- HP: 0000598
- HP: 0001159
- HP: 0001188
- HP: 0001250
- HP: 0001252
- HP: 0001382
- HP: 0001388
- HP: 0001508
- HP: 0001511
- HP: 0001622
- HP: 0001629
- HP: 0001631
- HP: 0001762
- HP: 0001770
- HP: 0001838
- HP: 0001941
- HP: 0002025
- HP: 0002098
- HP: 0002194
- HP: 0002260
- HP: 0002564
- HP: 0002884
- HP: 0003196
- HP: 0004322
- HP: 0004378
- HP: 0004383
- HP: 0010442
- HP: 0010862
- dbVar: nssv15148196
- dbVar: nssv15150633
- dbVar: nsv3907722
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.