nsv5364
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Yes
- Clinical Assertions: No
- Region Size:93,674
- 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: 2711 SVs from 101 studies. See in: genome view
Overlapping variant regions from other studies: 2711 SVs from 101 studies. See in: genome view
Overlapping variant regions from other studies: 736 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv5364 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 78,246,715 | 78,340,388 |
| nsv5364 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 78,956,432 | 79,050,105 |
| nsv5364 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000006.9 | Chr6 | 79,013,151 | 79,106,824 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3451 | Remapped | Perfect | NC_000006.12:g.(78 246715_?)_(?_78340 388)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 78,246,715 | 78,340,388 |
| nssv3451 | Remapped | Perfect | NC_000006.11:g.(78 956432_?)_(?_79050 105)del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 78,956,432 | 79,050,105 |
| nssv3451 | Submitted genomic | NC_000006.9:g.(790 13151_?)_(?_791068 24)del69513 | NCBI35 (hg17) | NC_000006.9 | Chr6 | 79,013,151 | 79,106,824 |