nsv932076 - (obsolete)
- Organism: Homo sapiens
- Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:33
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:2,772,244
- 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: nsv3901561
- ClinVar: SCV000181561
- ClinVar: SCV000502927
- ClinVar: SCV000502928
- HP: 0000122
- HP: 0000175
- HP: 0000176
- HP: 0000252
- HP: 0000271
- HP: 0000288
- HP: 0000347
- HP: 0000365
- HP: 0000431
- HP: 0000589
- HP: 0000598
- HP: 0000678
- HP: 0000722
- HP: 0000739
- HP: 0000750
- HP: 0000767
- HP: 0000776
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001256
- HP: 0001263
- HP: 0001276
- HP: 0001298
- HP: 0001305
- HP: 0001328
- HP: 0001371
- HP: 0001388
- HP: 0001508
- HP: 0001511
- HP: 0001513
- HP: 0001561
- HP: 0001622
- HP: 0001627
- HP: 0001628
- HP: 0001629
- HP: 0001636
- HP: 0001642
- HP: 0001660
- HP: 0001762
- HP: 0001873
- HP: 0002019
- HP: 0002063
- HP: 0002194
- HP: 0002260
- HP: 0002564
- HP: 0002715
- HP: 0002813
- HP: 0002870
- HP: 0002901
- HP: 0004313
- HP: 0004322
- HP: 0004383
- HP: 0005359
- HP: 0006482
- HP: 0007018
- HP: 0008551
- HP: 0010307
- HP: 0010862
- HP: 0011297
- HP: 0012418
- dbVar: nssv15139854
- dbVar: nssv15148769
- dbVar: nssv15150906
- dbVar: nsv3901561
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.