nsv529715 - (obsolete)
- Organism: Homo sapiens
- Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:10
- Validation:Yes
- Clinical Assertions: Yes
- Region Size:2,972,172
- 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: nsv3917963
- ClinVar: SCV000175367
- ClinVar: SCV000196333
- ClinVar: SCV000196334
- HP: 0000179
- HP: 0000215
- HP: 0000280
- HP: 0000316
- HP: 0000369
- HP: 0000565
- HP: 0000577
- HP: 0000687
- HP: 0000729
- HP: 0000739
- HP: 0000750
- HP: 0000821
- HP: 0000829
- HP: 0001250
- HP: 0001263
- HP: 0001328
- HP: 0001332
- HP: 0001385
- HP: 0001537
- HP: 0001622
- HP: 0001629
- HP: 0001999
- HP: 0002162
- HP: 0002194
- HP: 0002208
- HP: 0002345
- HP: 0002714
- HP: 0002901
- HP: 0004322
- HP: 0005280
- HP: 0030276
- dbVar: nssv15133393
- dbVar: nssv15133394
- dbVar: nsv4356850
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.