nsv932068 - (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:7
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:80,120,015
- 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: nsv3899451
- ClinVar: SCV000181551
- ClinVar: SCV000502926
- HP: 0000028
- HP: 0000369
- HP: 0000776
- HP: 0001252
- HP: 0001508
- HP: 0001511
- HP: 0001622
- HP: 0001636
- HP: 0002011
- HP: 0002032
- HP: 0002194
- HP: 0002260
- HP: 0002564
- HP: 0006610
- dbVar: nssv15148237
- dbVar: nssv15149221
- dbVar: nsv3899451
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.