nsv2769532 - (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:5
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:95,480,112
- 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: nsv3897712
- ClinVar: SCV000584439
- ClinVar: SCV000584440
- HP: 0000252
- HP: 0000271
- HP: 0000347
- HP: 0000589
- HP: 0000598
- HP: 0000776
- HP: 0001057
- HP: 0001159
- HP: 0001249
- HP: 0001252
- HP: 0001508
- HP: 0001511
- HP: 0001518
- HP: 0001561
- HP: 0001629
- HP: 0002119
- HP: 0002194
- HP: 0002260
- HP: 0002564
- HP: 0004322
- HP: 0010442
- HP: 0010862
- dbVar: nssv15161661
- dbVar: nssv15161681
- dbVar: nsv3897712
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.