nsv1191912
- Organism: Homo sapiens
- Study:nstd113 (Polyak et al. 2015)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:352,159
- Publication(s):Polyak et al. 2015
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1477 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1477 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 576 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1191912 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 180,700,225 | 181,052,383 |
| nsv1191912 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 181,621,378 | 181,973,536 |
| nsv1191912 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 181,858,372 | 182,210,530 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv7472172 | copy number loss | 72604 | Oligo aCGH | Probe signal intensity | 5 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv7472172 | Remapped | Perfect | NC_000004.12:g.(?_ 180700225)_(181052 383_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 180,700,225 | 181,052,383 |
| nssv7472172 | Remapped | Perfect | NC_000004.11:g.(?_ 181621378)_(181973 536_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 181,621,378 | 181,973,536 |
| nssv7472172 | Submitted genomic | NC_000004.10:g.(?_ 181858372)_(182210 530_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 181,858,372 | 182,210,530 |