nsv2769210 - (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:7,120,720
- Description:Metaphase FISH studies using 16p and 16q subtelomere probes (Abbott Molecular) demonstrated that the duplicated 16q material resides on distal 16p, suggesting that this abnormal chromosome 16 may be a recombinant from a parental pericentromeric inversion.. 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: nsv3901802
This variant has been obsoleted and is no longer valid.