nsv819536
- 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:27,301
- 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: 371 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 371 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 146 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819536 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 37,166,326 | 37,193,626 |
| nsv819536 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 37,455,254 | 37,482,554 |
| nsv819536 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 37,495,260 | 37,522,560 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418916 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418916 | Remapped | Perfect | NC_000010.11:g.(37 166326_?)_(?_37193 626)ins? | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 37,166,326 | 37,193,626 |
| nssv1418916 | Remapped | Perfect | NC_000010.10:g.(37 455254_?)_(?_37482 554)ins? | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 37,455,254 | 37,482,554 |
| nssv1418916 | Submitted genomic | NC_000010.9:g.(374 95260_?)_(?_375225 60)ins(0_?) | NCBI36 (hg18) | NC_000010.9 | Chr10 | 37,495,260 | 37,522,560 |