nsv819182
- 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:108,201
- 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: 526 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 526 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 189 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819182 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 14,434,195 | 14,542,395 |
| nsv819182 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 14,434,194 | 14,542,394 |
| nsv819182 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 14,424,194 | 14,532,394 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418918 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418918 | Remapped | Perfect | NC_000018.10:g.(14 434195_?)_(?_14542 395)ins? | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 14,434,195 | 14,542,395 |
| nssv1418918 | Remapped | Perfect | NC_000018.9:g.(144 34194_?)_(?_145423 94)ins? | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 14,434,194 | 14,542,394 |
| nssv1418918 | Submitted genomic | NC_000018.8:g.(144 24194_?)_(?_145323 94)ins(0_?) | NCBI36 (hg18) | NC_000018.8 | Chr18 | 14,424,194 | 14,532,394 |