nsv931114 - (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:34
- 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: nsv3922647
- ClinVar: SCV000180613
- ClinVar: SCV000180614
- HP: 0000028
- HP: 0000047
- HP: 0000122
- HP: 0000126
- HP: 0000160
- HP: 0000175
- HP: 0000204
- HP: 0000218
- HP: 0000252
- HP: 0000271
- HP: 0000276
- HP: 0000286
- HP: 0000316
- HP: 0000347
- HP: 0000478
- HP: 0000581
- HP: 0000598
- HP: 0000708
- HP: 0000716
- HP: 0000717
- HP: 0000750
- HP: 0000954
- HP: 0001007
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001263
- HP: 0001281
- HP: 0001298
- HP: 0001328
- HP: 0001508
- HP: 0001511
- HP: 0001601
- HP: 0001622
- HP: 0001629
- HP: 0001631
- HP: 0001636
- HP: 0001642
- HP: 0001660
- HP: 0002098
- HP: 0002260
- HP: 0002474
- HP: 0002564
- HP: 0002714
- HP: 0002808
- HP: 0002901
- HP: 0003468
- HP: 0004404
- HP: 0004937
- HP: 0006870
- HP: 0011333
- dbVar: nssv15137698
- dbVar: nssv15138712
- dbVar: nsv4353568
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.