nsv831433
- 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:206,301
- 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: 691 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 697 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 63 SVs from 5 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv831433 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 116,037,550 | 116,243,850 |
| nsv831433 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 117,049,775 | 117,256,088 |
| nsv831433 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 117,118,953 | 117,325,269 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1447437 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1447438 | copy number loss | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1447437 | Remapped | Good | NC_000008.11:g.(11 6037550_?)_(?_1162 43850)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 116,037,550 | 116,243,850 |
| nssv1447438 | Remapped | Good | NC_000008.11:g.(11 6037550_?)_(?_1162 43850)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 116,037,550 | 116,243,850 |
| nssv1447437 | Remapped | Good | NC_000008.10:g.(11 7049775_?)_(?_1172 56088)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 117,049,775 | 117,256,088 |
| nssv1447438 | Remapped | Good | NC_000008.10:g.(11 7049775_?)_(?_1172 56088)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 117,049,775 | 117,256,088 |
| nssv1447437 | Submitted genomic | NC_000008.9:g.(117 118953_?)_(?_11732 5269)del | NCBI35 (hg17) | NC_000008.9 | Chr8 | 117,118,953 | 117,325,269 | ||
| nssv1447438 | Submitted genomic | NC_000008.9:g.(117 118953_?)_(?_11732 5269)del | NCBI35 (hg17) | NC_000008.9 | Chr8 | 117,118,953 | 117,325,269 |