nsv1191881
- 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:425,587
- 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: 1270 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 1271 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 396 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1191881 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 124,033,715 | 124,459,301 |
| nsv1191881 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 124,354,860 | 124,780,447 |
| nsv1191881 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 124,396,559 | 124,822,146 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv7472142 | copy number gain | 61152 | Oligo aCGH | Probe signal intensity | nssv7465968, nssv7468431 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv7472142 | Remapped | Perfect | NC_000006.12:g.(?_ 124033715)_(124459 301_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 124,033,715 | 124,459,301 |
| nssv7472142 | Remapped | Perfect | NC_000006.11:g.(?_ 124354860)_(124780 447_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 124,354,860 | 124,780,447 |
| nssv7472142 | Submitted genomic | NC_000006.10:g.(?_ 124396559)_(124822 146_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 124,396,559 | 124,822,146 |