nsv529813 - (obsolete)
- Organism: Homo sapiens
- Study:nstd101 (obsolete - ClinGen Kaminsky et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:9
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:2,923,482
- 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):Kaminsky et al. 2011
- Replacement Description: Replaced nstd101 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Replacement Variant: nsv3922286
- ClinVar: SCV000078622
- ClinVar: SCV000078623
- HP: 0000126
- HP: 0000175
- HP: 0000252
- HP: 0000717
- HP: 0001250
- HP: 0001252
- HP: 0001263
- HP: 0001264
- HP: 0001508
- HP: 0001511
- HP: 0001627
- HP: 0001674
- HP: 0001999
- HP: 0002317
- HP: 0002463
- HP: 0002779
- HP: 0004322
- HP: 0008787
- dbVar: nssv15132127
- dbVar: nssv15133434
- dbVar: nsv4355323
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.