nsv832508
- Organism: Homo sapiens
- Study:nstd68 (Wong et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:210,316
- 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: 438 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 438 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv832508 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 105,805,019 | 106,015,334 |
| nsv832508 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 106,198,797 | 106,409,112 |
| nsv832508 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000012.9 | Chr12 | 104,701,264 | 104,911,579 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1449997 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1449998 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1449997 | Remapped | Perfect | NC_000012.12:g.(10 5805019_?)_(?_1060 15334)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 105,805,019 | 106,015,334 |
| nssv1449998 | Remapped | Perfect | NC_000012.12:g.(10 5805019_?)_(?_1060 15334)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 105,805,019 | 106,015,334 |
| nssv1449997 | Remapped | Perfect | NC_000012.11:g.(10 6198797_?)_(?_1064 09112)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 106,198,797 | 106,409,112 |
| nssv1449998 | Remapped | Perfect | NC_000012.11:g.(10 6198797_?)_(?_1064 09112)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 106,198,797 | 106,409,112 |
| nssv1449997 | Submitted genomic | NC_000012.9:g.(104 701264_?)_(?_10491 1579)dup | NCBI35 (hg17) | NC_000012.9 | Chr12 | 104,701,264 | 104,911,579 | ||
| nssv1449998 | Submitted genomic | NC_000012.9:g.(104 701264_?)_(?_10491 1579)dup | NCBI35 (hg17) | NC_000012.9 | Chr12 | 104,701,264 | 104,911,579 |