nsv819550
- 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:42
- 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: 143 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 143 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 31 SVs from 12 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819550 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 33,458,789 | 33,458,830 |
| nsv819550 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 33,949,695 | 33,949,736 |
| nsv819550 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 38,641,535 | 38,641,576 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418902 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418902 | Remapped | Perfect | NC_000019.10:g.(33 458789_?)_(?_33458 830)ins1058 | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 33,458,789 | 33,458,830 |
| nssv1418902 | Remapped | Perfect | NC_000019.9:g.(339 49695_?)_(?_339497 36)ins1058 | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 33,949,695 | 33,949,736 |
| nssv1418902 | Submitted genomic | NC_000019.8:g.(386 41535_?)_(?_386415 76)ins1058 | NCBI36 (hg18) | NC_000019.8 | Chr19 | 38,641,535 | 38,641,576 |