nsv915674 - (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:10
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:3,862,457
- 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: nsv3899666
- ClinVar: SCV000178759
- ClinVar: SCV000178761
- HP: 0000586
- HP: 0000708
- HP: 0000729
- HP: 0000750
- HP: 0001250
- HP: 0001263
- HP: 0001290
- HP: 0001328
- HP: 0001360
- HP: 0001999
- HP: 0002072
- HP: 0002099
- HP: 0002194
- HP: 0006610
- HP: 0007099
- HP: 0010862
- HP: 0040083
- HP: 0100629
- dbVar: nssv15135517
- dbVar: nssv15135832
- dbVar: nsv4359223
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.