nsv957757
- Organism: Homo sapiens
- Study:nstd73 (Dogan et al. 2014)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:148
- Publication(s):Dogan et al. 2014
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: 152 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 152 SVs from 38 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv957757 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 94,312,905 | 94,313,052 |
| nsv957757 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 97,075,187 | 97,075,334 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3002363 | insertion | SAMN01096093 | Sequencing | Paired-end mapping | 9,109 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3002363 | Remapped | Perfect | NC_000009.12:g.(94 312905_?)_(?_94313 052)ins? | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 94,312,905 | 94,313,052 |
| nssv3002363 | Submitted genomic | NC_000009.11:g.(97 075187_?)_(?_97075 334)ins(0_?) | GRCh37 (hg19) | NC_000009.11 | Chr9 | 97,075,187 | 97,075,334 |