nsv3088
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:10,429
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 154 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 160 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 5 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3088 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 156,710,832 | 156,721,260 |
| nsv3088 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 156,680,624 | 156,691,052 |
| nsv3088 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 153,493,697 | 153,504,125 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv7706 | Remapped | Perfect | NC_000001.11:g.(15 6710832_?)_(?_1567 21260)ins5824 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 156,710,832 | 156,721,260 |
| nssv7706 | Remapped | Perfect | NC_000001.10:g.(15 6680624_?)_(?_1566 91052)ins5824 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 156,680,624 | 156,691,052 |
| nssv7706 | Submitted genomic | NC_000001.8:g.(153 493697_?)_(?_15350 4125)ins5824 | NCBI35 (hg17) | NC_000001.8 | Chr1 | 153,493,697 | 153,504,125 |