nsv3538370
- Organism: Homo sapiens
- Study:nstd152 (Chaisson et al. 2019)
- Variant Type:mobile element insertion
- Method Type:Optical mapping, Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:Insertion of a HERV mobile element relative to the reference
- Publication(s):Chaisson et al. 2019
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: 138 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3538370 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 118,486,551 | 118,486,551 | ||
| nsv3538370 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 121,248,829 | 121,248,829 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14428926 | herv insertion | HG00514 | Optical mapping, Sequencing | Optical mapping, Sequence alignment, de novo and local sequence assembly | 39,861 |
| nssv14467392 | herv insertion | SAMN00006581 | Optical mapping, Sequencing | Optical mapping, Sequence alignment, de novo and local sequence assembly | 41,185 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14428926 | Submitted genomic | NC_000009.12:g.118 486551_118486552in s199 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 118,486,551 | 118,486,551 | ||
| nssv14467392 | Submitted genomic | NC_000009.12:g.118 486551_118486552in s199 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 118,486,551 | 118,486,551 | ||
| nssv14428926 | Remapped | Perfect | NC_000009.11:g.121 248829_121248830in s199 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 121,248,829 | 121,248,829 |
| nssv14467392 | Remapped | Perfect | NC_000009.11:g.121 248829_121248830in s199 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 121,248,829 | 121,248,829 |