nsv436043
- 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:9,486
- 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: 538 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 538 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 202 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv436043 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 122,581,663 | 122,591,148 |
| nsv436043 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 124,341,179 | 124,350,664 |
| nsv436043 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 124,331,169 | 124,340,654 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv466621 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv466621 | Remapped | Perfect | NC_000010.11:g.(12 2581663_?)_(?_1225 91148)ins? | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 122,581,663 | 122,591,148 |
| nssv466621 | Remapped | Perfect | NC_000010.10:g.(12 4341179_?)_(?_1243 50664)ins? | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 124,341,179 | 124,350,664 |
| nssv466621 | Submitted genomic | NC_000010.9:g.(124 331169_?)_(?_12434 0654)ins(0_?) | NCBI36 (hg18) | NC_000010.9 | Chr10 | 124,331,169 | 124,340,654 |