nsv958012
- 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:157
- 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: 127 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 127 SVs from 26 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv958012 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 42,557,405 | 42,557,561 |
| nsv958012 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 42,849,603 | 42,849,759 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3005544 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3005544 | Remapped | Perfect | NC_000015.10:g.(42 557405_?)_(?_42557 561)ins? | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 42,557,405 | 42,557,561 |
| nssv3005544 | Submitted genomic | NC_000015.9:g.(428 49603_?)_(?_428497 59)ins(0_?) | GRCh37 (hg19) | NC_000015.9 | Chr15 | 42,849,603 | 42,849,759 |