nsv482253
- 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:221,325
- 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: 926 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 957 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 4 SVs from 1 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482253 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 64,476,875 | 64,698,199 |
| nsv482253 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 69,489,293 | 69,710,617 |
| nsv482253 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | GPC_000000201.1 | Chr9 | 65,619,734 | 65,841,058 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3009330 | sequence alteration | BAC aCGH | Probe signal intensity |
| nssv3010193 | sequence alteration | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3009330 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 64,476,875 | 64,698,199 |
| nssv3010193 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 64,476,875 | 64,698,199 |
| nssv3009330 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 69,489,293 | 69,710,617 |
| nssv3010193 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 69,489,293 | 69,710,617 |
| nssv3009330 | Submitted genomic | NCBI34 (hg16) | GPC_000000201.1 | Chr9 | 65,619,734 | 65,841,058 | ||
| nssv3010193 | Submitted genomic | NCBI34 (hg16) | GPC_000000201.1 | Chr9 | 65,619,734 | 65,841,058 |