nsv436063
- 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:11,218
- 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: 171 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 171 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 60 SVs from 13 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv436063 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 9,354,796 | 9,366,013 |
| nsv436063 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 9,258,113 | 9,269,330 |
| nsv436063 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 9,198,838 | 9,210,055 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv465586 | insertion | SAMN00000376 | Sequencing | Paired-end mapping | 468 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv465586 | Remapped | Perfect | NC_000017.11:g.(93 54796_?)_(?_936601 3)ins? | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 9,354,796 | 9,366,013 |
| nssv465586 | Remapped | Perfect | NC_000017.10:g.(92 58113_?)_(?_926933 0)ins? | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 9,258,113 | 9,269,330 |
| nssv465586 | Submitted genomic | NC_000017.9:g.(919 8838_?)_(?_9210055 )ins(0_?) | NCBI36 (hg18) | NC_000017.9 | Chr17 | 9,198,838 | 9,210,055 |