nsv995375 - (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:155,752,188
- 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: nsv3887722
- ClinVar: SCV000182799
- ClinVar: SCV000182800
- ClinVar: SCV000502947
- ClinVar: SCV000502948
- ClinVar: SCV000502949
- HP: 0000237
- HP: 0000252
- HP: 0000271
- HP: 0000316
- HP: 0000347
- HP: 0000369
- HP: 0000431
- HP: 0000470
- HP: 0000525
- HP: 0000581
- HP: 0000598
- HP: 0000601
- HP: 0000717
- HP: 0000729
- HP: 0000750
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001263
- HP: 0001307
- HP: 0001328
- HP: 0001508
- HP: 0001509
- HP: 0001511
- HP: 0001548
- HP: 0001627
- HP: 0001631
- HP: 0001651
- HP: 0002007
- HP: 0002032
- HP: 0002117
- HP: 0002194
- HP: 0002260
- HP: 0002311
- HP: 0002575
- HP: 0002650
- HP: 0002714
- HP: 0006905
- HP: 0007228
- HP: 0010566
- HP: 0010862
- HP: 0011662
- dbVar: nssv15161576
- dbVar: nssv15161635
- dbVar: nssv15161641
- dbVar: nssv15161648
- dbVar: nssv15161811
- dbVar: nsv3887722
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.