nsv436416
- Organism: Homo sapiens
- Study:nstd16 (Korbel et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Yes
- Clinical Assertions: No
- Region Size:131,669
- Publication(s):Korbel et al. 2007
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: 506 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 506 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 164 SVs from 18 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv436416 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 166,970,976 | 167,102,644 |
| nsv436416 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 167,892,127 | 168,023,795 |
| nsv436416 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 168,128,702 | 168,260,370 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv466168 | deletion | SAMN00001583 | Sequencing | Paired-end mapping | 822 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv466168 | Remapped | Perfect | NC_000004.12:g.(16 6970976_?)_(?_1671 02644)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 166,970,976 | 167,102,644 |
| nssv466168 | Remapped | Perfect | NC_000004.11:g.(16 7892127_?)_(?_1680 23795)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 167,892,127 | 168,023,795 |
| nssv466168 | Submitted genomic | NC_000004.10:g.(16 8128702_?)_(?_1682 60370)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 168,128,702 | 168,260,370 |
Validation Information
| Variant Call ID | Experiment ID | Sample ID | Method | Analysis | Result |
|---|---|---|---|---|---|
| nssv466168 | 4 | SAMN00001583 | PCR | Manual observation | Pass |