nsv436914
- Organism: Homo sapiens
- Study:nstd16 (Korbel et al. 2007)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:17,856
- Description:Unmated-Insertion
- 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: 335 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 341 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 169 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv436914 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 17,927,608 | 17,945,463 |
| nsv436914 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 17,927,606 | 17,945,461 |
| nsv436914 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 17,917,606 | 17,935,461 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv466508 | insertion | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv466508 | Remapped | Perfect | NC_000009.12:g.(17 927608_?)_(?_17945 463)ins? | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,927,608 | 17,945,463 |
| nssv466508 | Remapped | Perfect | NC_000009.11:g.(17 927606_?)_(?_17945 461)ins? | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 17,927,606 | 17,945,461 |
| nssv466508 | Submitted genomic | NC_000009.10:g.(17 917606_?)_(?_17935 461)ins(0_?) | NCBI36 (hg18) | NC_000009.10 | Chr9 | 17,917,606 | 17,935,461 |