nsv831929
- Organism: Homo sapiens
- Study:nstd68 (Wong et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:218,402
- Publication(s):Wong 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: 675 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 675 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 24 SVs from 6 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv831929 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 83,208,549 | 83,426,950 |
| nsv831929 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 84,968,305 | 85,186,706 |
| nsv831929 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 84,958,285 | 85,176,686 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1448626 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1448627 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1448630 | copy number gain | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1448626 | Remapped | Perfect | NC_000010.11:g.(83 208549_?)_(?_83426 950)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 83,208,549 | 83,426,950 |
| nssv1448627 | Remapped | Perfect | NC_000010.11:g.(83 208549_?)_(?_83426 950)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 83,208,549 | 83,426,950 |
| nssv1448630 | Remapped | Perfect | NC_000010.11:g.(83 208549_?)_(?_83426 950)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 83,208,549 | 83,426,950 |
| nssv1448626 | Remapped | Perfect | NC_000010.10:g.(84 968305_?)_(?_85186 706)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 84,968,305 | 85,186,706 |
| nssv1448627 | Remapped | Perfect | NC_000010.10:g.(84 968305_?)_(?_85186 706)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 84,968,305 | 85,186,706 |
| nssv1448630 | Remapped | Perfect | NC_000010.10:g.(84 968305_?)_(?_85186 706)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 84,968,305 | 85,186,706 |
| nssv1448626 | Submitted genomic | NC_000010.8:g.(849 58285_?)_(?_851766 86)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 84,958,285 | 85,176,686 | ||
| nssv1448627 | Submitted genomic | NC_000010.8:g.(849 58285_?)_(?_851766 86)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 84,958,285 | 85,176,686 | ||
| nssv1448630 | Submitted genomic | NC_000010.8:g.(849 58285_?)_(?_851766 86)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 84,958,285 | 85,176,686 |