nsv995205 - (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:75
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:33,043,324
- 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: nsv3908402
- ClinVar: SCV000182621
- ClinVar: SCV000586667
- HP: 0000047
- HP: 0000126
- HP: 0000158
- HP: 0000175
- HP: 0000204
- HP: 0000252
- HP: 0000271
- HP: 0000286
- HP: 0000316
- HP: 0000347
- HP: 0000369
- HP: 0000431
- HP: 0000464
- HP: 0000465
- HP: 0000470
- HP: 0000474
- HP: 0000541
- HP: 0000568
- HP: 0000582
- HP: 0000598
- HP: 0000733
- HP: 0000750
- HP: 0001159
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001257
- HP: 0001263
- HP: 0001392
- HP: 0001508
- HP: 0001511
- HP: 0001537
- HP: 0001560
- HP: 0001622
- HP: 0001627
- HP: 0001629
- HP: 0001631
- HP: 0001636
- HP: 0001641
- HP: 0001643
- HP: 0001655
- HP: 0001674
- HP: 0001762
- HP: 0001852
- HP: 0001869
- HP: 0001873
- HP: 0001901
- HP: 0002009
- HP: 0002020
- HP: 0002089
- HP: 0002098
- HP: 0002170
- HP: 0002194
- HP: 0002247
- HP: 0002260
- HP: 0002564
- HP: 0002591
- HP: 0002813
- HP: 0004322
- HP: 0004453
- HP: 0005257
- HP: 0005753
- HP: 0005989
- HP: 0006610
- HP: 0006721
- HP: 0007598
- HP: 0009161
- HP: 0010442
- HP: 0010808
- HP: 0010862
- HP: 0030148
- HP: 0100703
- HP: 0100806
- dbVar: nssv15149002
- dbVar: nssv15150236
- dbVar: nsv3908402
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.