nsv995182 - (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:3
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:86,833,716
- 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: nsv3904265
- ClinVar: SCV000182598
- ClinVar: SCV000586665
- HP: 0000278
- HP: 0000347
- HP: 0000365
- HP: 0000598
- HP: 0000952
- HP: 0001159
- HP: 0001511
- HP: 0001629
- HP: 0001852
- HP: 0001873
- HP: 0002260
- HP: 0002564
- HP: 0004322
- HP: 0008070
- HP: 0010442
- HP: 0011329
- HP: 0100257
- dbVar: nssv15161107
- dbVar: nssv15161424
- dbVar: nsv3904265
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.