nsv482670
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:sequence alteration
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:196,459
- Publication(s):Sharp et al. 2006
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: 789 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 789 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 2 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482670 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 7,096,161 | 7,292,619 |
| nsv482670 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 7,135,792 | 7,332,250 |
| nsv482670 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000007.10 | Chr7 | 6,880,129 | 7,076,587 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3006338 | sequence alteration | BAC aCGH | Probe signal intensity |
| nssv3007924 | sequence alteration | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3006338 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 7,096,161 | 7,292,619 |
| nssv3007924 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 7,096,161 | 7,292,619 |
| nssv3006338 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 7,135,792 | 7,332,250 |
| nssv3007924 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 7,135,792 | 7,332,250 |
| nssv3006338 | Submitted genomic | NCBI34 (hg16) | NC_000007.10 | Chr7 | 6,880,129 | 7,076,587 | ||
| nssv3007924 | Submitted genomic | NCBI34 (hg16) | NC_000007.10 | Chr7 | 6,880,129 | 7,076,587 |