nsv491969 - (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:26
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:2,811,999
- 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: nsv3910011
- ClinVar: SCV000173304
- ClinVar: SCV000173306
- ClinVar: SCV000196183
- ClinVar: SCV000196184
- HP: 0000047
- HP: 0000175
- HP: 0000252
- HP: 0000369
- HP: 0000729
- HP: 0000750
- HP: 0000921
- HP: 0001252
- HP: 0001263
- HP: 0001290
- HP: 0001328
- HP: 0001508
- HP: 0001511
- HP: 0001562
- HP: 0001622
- HP: 0001636
- HP: 0001702
- HP: 0001999
- HP: 0002023
- HP: 0002194
- HP: 0002260
- HP: 0004322
- HP: 0005359
- HP: 0007018
- HP: 0010862
- HP: 0011469
- HP: 0011611
- HP: 0030148
- HP: 0100543
- dbVar: nssv15131931
- dbVar: nssv15133075
- dbVar: nssv15133317
- dbVar: nsv4353698
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.