nsv436669
- Organism: Homo sapiens
- Study:nstd16 (Korbel et al. 2007)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Yes
- Clinical Assertions: No
- Region Size:7,427
- 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: 303 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 303 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 134 SVs from 23 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv436669 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 179,543,896 | 179,551,322 |
| nsv436669 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 180,408,623 | 180,416,049 |
| nsv436669 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 180,116,868 | 180,124,294 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv465961 | inversion | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv465961 | Remapped | Perfect | NC_000002.12:g.(17 9543896_?)_(?_1795 51322)inv | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 179,543,896 | 179,551,322 |
| nssv465961 | Remapped | Perfect | NC_000002.11:g.(18 0408623_?)_(?_1804 16049)inv | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 180,408,623 | 180,416,049 |
| nssv465961 | Submitted genomic | NC_000002.10:g.(18 0116868_?)_(?_1801 24294)inv | NCBI36 (hg18) | NC_000002.10 | Chr2 | 180,116,868 | 180,124,294 |
Validation Information
| Variant Call ID | Experiment ID | Sample ID | Method | Analysis | Result |
|---|---|---|---|---|---|
| nssv465961 | 4 | SAMN00001583 | PCR | Manual observation | Pass |