nsv995341 - (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:1
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:81,319,452
- Description:unbalanced X;16 translocation. 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: nsv3902810
- ClinVar: SCV000182765
- HP: 0000175
- HP: 0000252
- HP: 0000545
- HP: 0000577
- HP: 0000750
- HP: 0000767
- HP: 0000776
- HP: 0000792
- HP: 0000953
- HP: 0001249
- HP: 0001250
- HP: 0001252
- HP: 0001257
- HP: 0001288
- HP: 0001508
- HP: 0001511
- HP: 0002020
- HP: 0002088
- HP: 0002119
- HP: 0002194
- HP: 0002260
- HP: 0002650
- HP: 0004322
- HP: 0005280
- HP: 0010862
- dbVar: nssv15161575
- dbVar: nsv4348604
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.