nsv492017 - (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:50
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:155,992,542
- 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: nsv3897404
- ClinVar: SCV000173365
- ClinVar: SCV000173367
- ClinVar: SCV000173368
- HP: 0000028
- HP: 0000085
- HP: 0000133
- HP: 0000185
- HP: 0000202
- HP: 0000252
- HP: 0000271
- HP: 0000365
- HP: 0000476
- HP: 0000508
- HP: 0000708
- HP: 0000717
- HP: 0000729
- HP: 0000735
- HP: 0000750
- HP: 0000752
- HP: 0000802
- HP: 0001155
- HP: 0001249
- HP: 0001252
- HP: 0001263
- HP: 0001276
- HP: 0001290
- HP: 0001298
- HP: 0001328
- HP: 0001508
- HP: 0001510
- HP: 0001511
- HP: 0001562
- HP: 0001622
- HP: 0001629
- HP: 0001650
- HP: 0001714
- HP: 0001763
- HP: 0001999
- HP: 0002084
- HP: 0002194
- HP: 0002260
- HP: 0002650
- HP: 0003198
- HP: 0004322
- HP: 0004482
- HP: 0005235
- HP: 0006610
- HP: 0009830
- HP: 0010862
- HP: 0012098
- HP: 0030853
- HP: 0100033
- HP: 0100704
- HP: 0100785
- dbVar: nssv15161309
- dbVar: nssv15161527
- dbVar: nsv4353057
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.