nsv832551
- Organism: Homo sapiens
- Study:nstd68 (Wong et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:7
- Validation:Not tested
- Clinical Assertions: No
- Region Size:206,060
- 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: 906 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 906 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 41 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv832551 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nsv832551 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nsv832551 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1450082 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1450083 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1450085 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1450086 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1450087 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1450088 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1450089 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1450082 | Remapped | Perfect | NC_000012.12:g.(12 9721471_?)_(?_1299 27530)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nssv1450083 | Remapped | Perfect | NC_000012.12:g.(12 9721471_?)_(?_1299 27530)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nssv1450085 | Remapped | Perfect | NC_000012.12:g.(12 9721471_?)_(?_1299 27530)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nssv1450086 | Remapped | Perfect | NC_000012.12:g.(12 9721471_?)_(?_1299 27530)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nssv1450087 | Remapped | Perfect | NC_000012.12:g.(12 9721471_?)_(?_1299 27530)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nssv1450088 | Remapped | Perfect | NC_000012.12:g.(12 9721471_?)_(?_1299 27530)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nssv1450089 | Remapped | Perfect | NC_000012.12:g.(12 9721471_?)_(?_1299 27530)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 129,721,471 | 129,927,530 |
| nssv1450082 | Remapped | Perfect | NC_000012.11:g.(13 0206016_?)_(?_1304 12075)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nssv1450083 | Remapped | Perfect | NC_000012.11:g.(13 0206016_?)_(?_1304 12075)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nssv1450085 | Remapped | Perfect | NC_000012.11:g.(13 0206016_?)_(?_1304 12075)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nssv1450086 | Remapped | Perfect | NC_000012.11:g.(13 0206016_?)_(?_1304 12075)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nssv1450087 | Remapped | Perfect | NC_000012.11:g.(13 0206016_?)_(?_1304 12075)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nssv1450088 | Remapped | Perfect | NC_000012.11:g.(13 0206016_?)_(?_1304 12075)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nssv1450089 | Remapped | Perfect | NC_000012.11:g.(13 0206016_?)_(?_1304 12075)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 130,206,016 | 130,412,075 |
| nssv1450082 | Submitted genomic | NC_000012.9:g.(128 730896_?)_(?_12893 6955)del | NCBI35 (hg17) | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 | ||
| nssv1450083 | Submitted genomic | NC_000012.9:g.(128 730896_?)_(?_12893 6955)del | NCBI35 (hg17) | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 | ||
| nssv1450085 | Submitted genomic | NC_000012.9:g.(128 730896_?)_(?_12893 6955)del | NCBI35 (hg17) | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 | ||
| nssv1450086 | Submitted genomic | NC_000012.9:g.(128 730896_?)_(?_12893 6955)del | NCBI35 (hg17) | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 | ||
| nssv1450087 | Submitted genomic | NC_000012.9:g.(128 730896_?)_(?_12893 6955)del | NCBI35 (hg17) | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 | ||
| nssv1450088 | Submitted genomic | NC_000012.9:g.(128 730896_?)_(?_12893 6955)del | NCBI35 (hg17) | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 | ||
| nssv1450089 | Submitted genomic | NC_000012.9:g.(128 730896_?)_(?_12893 6955)del | NCBI35 (hg17) | NC_000012.9 | Chr12 | 128,730,896 | 128,936,955 |