nsv497803 - (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:45
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:1,348,331
- 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: nsv3911924
- ClinVar: SCV000174299
- ClinVar: SCV000174300
- HP: 0000126
- HP: 0000152
- HP: 0000175
- HP: 0000256
- HP: 0000277
- HP: 0000280
- HP: 0000286
- HP: 0000301
- HP: 0000365
- HP: 0000707
- HP: 0000708
- HP: 0000717
- HP: 0000750
- HP: 0000769
- HP: 0000826
- HP: 0001155
- HP: 0001176
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001263
- HP: 0001270
- HP: 0001276
- HP: 0001328
- HP: 0001513
- HP: 0001622
- HP: 0001999
- HP: 0002260
- HP: 0004322
- HP: 0007018
- HP: 0008936
- HP: 0010311
- HP: 0100021
- dbVar: nssv15132758
- dbVar: nssv15138995
- dbVar: nsv4350993
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.