nsv820485
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,248
- Publication(s):Ju et al. 2010
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: 554 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 554 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 372 SVs from 24 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv820485 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 179,197,015 | 179,218,262 |
| nsv820485 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 180,061,742 | 180,082,989 |
| nsv820485 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 179,769,987 | 179,791,234 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420279 | Remapped | Perfect | NC_000002.12:g.(?_ 179197015)_(179218 262_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 179,197,015 | 179,218,262 |
| nssv1420279 | Remapped | Perfect | NC_000002.11:g.(?_ 180061742)_(180082 989_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 180,061,742 | 180,082,989 |
| nssv1420279 | Submitted genomic | NC_000002.10:g.(?_ 179769987)_(179791 234_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 179,769,987 | 179,791,234 |