nsv819703
- 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:229
- 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: 144 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 53 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819703 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 86,053,324 | 86,053,552 |
| nsv819703 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 88,668,239 | 88,668,467 |
| nsv819703 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 87,858,059 | 87,858,287 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418895 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418895 | Remapped | Perfect | NC_000009.12:g.(86 053324_?)_(?_86053 552)ins1129 | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 86,053,324 | 86,053,552 |
| nssv1418895 | Remapped | Perfect | NC_000009.11:g.(88 668239_?)_(?_88668 467)ins1129 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 88,668,239 | 88,668,467 |
| nssv1418895 | Submitted genomic | NC_000009.10:g.(87 858059_?)_(?_87858 287)ins1129 | NCBI36 (hg18) | NC_000009.10 | Chr9 | 87,858,059 | 87,858,287 |