nsv915550 - (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:18
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:540,658
- 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: nsv3924824
- ClinVar: SCV000178620
- ClinVar: SCV000178622
- HP: 0000077
- HP: 0000202
- HP: 0000729
- HP: 0000750
- HP: 0001249
- HP: 0001250
- HP: 0001263
- HP: 0001382
- HP: 0001513
- HP: 0001562
- HP: 0001999
- HP: 0002194
- HP: 0007360
- HP: 0011304
- HP: 0030148
- HP: 0100543
- dbVar: nssv15135477
- dbVar: nssv15136075
- dbVar: nsv4359416
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.