nsv932069 - (obsolete)
- Organism: Homo sapiens
- Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:62
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:155,752,187
- 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: nsv3874546
- ClinVar: SCV000181552
- ClinVar: SCV000181553
- ClinVar: SCV000181554
- ClinVar: SCV000586662
- HP: 0000044
- HP: 0000054
- HP: 0000057
- HP: 0000062
- HP: 0000133
- HP: 0000141
- HP: 0000158
- HP: 0000175
- HP: 0000204
- HP: 0000234
- HP: 0000252
- HP: 0000256
- HP: 0000268
- HP: 0000271
- HP: 0000278
- HP: 0000347
- HP: 0000508
- HP: 0000598
- HP: 0000657
- HP: 0000708
- HP: 0000717
- HP: 0000739
- HP: 0000750
- HP: 0000855
- HP: 0001159
- HP: 0001249
- HP: 0001250
- HP: 0001251
- HP: 0001252
- HP: 0001256
- HP: 0001260
- HP: 0001263
- HP: 0001276
- HP: 0001298
- HP: 0001328
- HP: 0001508
- HP: 0001511
- HP: 0001513
- HP: 0001518
- HP: 0001537
- HP: 0001548
- HP: 0001622
- HP: 0001629
- HP: 0001643
- HP: 0001674
- HP: 0001680
- HP: 0001696
- HP: 0001762
- HP: 0001845
- HP: 0001849
- HP: 0002025
- HP: 0002089
- HP: 0002098
- HP: 0002099
- HP: 0002194
- HP: 0002260
- HP: 0002323
- HP: 0002564
- HP: 0002650
- HP: 0002813
- HP: 0002884
- HP: 0003083
- HP: 0004322
- HP: 0004383
- HP: 0005692
- HP: 0007018
- HP: 0007429
- HP: 0007598
- HP: 0007973
- HP: 0008551
- HP: 0008720
- HP: 0010442
- HP: 0010734
- HP: 0011800
- HP: 0012098
- HP: 0100807
- dbVar: nssv15161092
- dbVar: nssv15161346
- dbVar: nssv15161682
- dbVar: nssv15161806
- dbVar: nsv3874546
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.