nsv513418
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,595
- Publication(s):Arlt et al. 2011
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: 166 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 54 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv513418 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 97,787,183 | 97,788,777 |
| nsv513418 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 98,253,520 | 98,255,114 |
| nsv513418 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 97,323,273 | 97,324,867 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv625816 | insertion | 1 | Sequencing | Paired-end mapping | 2,637 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv625816 | Remapped | Perfect | NC_000014.9:g.(977 87183_?)_(?_977887 77)ins891 | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 97,787,183 | 97,788,777 |
| nssv625816 | Remapped | Perfect | NC_000014.8:g.(982 53520_?)_(?_982551 14)ins891 | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 98,253,520 | 98,255,114 |
| nssv625816 | Submitted genomic | NC_000014.7:g.(973 23273_?)_(?_973248 67)ins891 | NCBI36 (hg18) | NC_000014.7 | Chr14 | 97,323,273 | 97,324,867 |