nsv819010
- Organism: Homo sapiens
- Study:nstd43 (Kim et al. 2009)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:35
- Publication(s):Kim et al. 2009
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: 442 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 441 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 233 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819010 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 150,417,903 | 150,417,937 |
| nsv819010 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 149,586,177 | 149,586,211 |
| nsv819010 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 149,336,835 | 149,336,869 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418909 | insertion | SAMN00002681 | Sequencing | Paired-end mapping | 1,333 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418909 | Remapped | Perfect | NC_000023.11:g.(15 0417903_?)_(?_1504 17937)ins1856 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 150,417,903 | 150,417,937 |
| nssv1418909 | Remapped | Perfect | NC_000023.10:g.(14 9586177_?)_(?_1495 86211)ins1856 | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 149,586,177 | 149,586,211 |
| nssv1418909 | Submitted genomic | NC_000023.9:g.(149 336835_?)_(?_14933 6869)ins1856 | NCBI36 (hg18) | NC_000023.9 | ChrX | 149,336,835 | 149,336,869 |