nsv482610
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:7
- Validation:Not tested
- Clinical Assertions: No
- Region Size:157,965
- 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: 443 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 443 SVs from 54 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482610 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nsv482610 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nsv482610 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3006533 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3006814 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3008596 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3008887 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3009564 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3009813 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3010233 | copy number loss | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3006533 | Remapped | Perfect | NC_000017.11:g.(?_ 65218252)_(6537621 6_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nssv3006814 | Remapped | Perfect | NC_000017.11:g.(?_ 65218252)_(6537621 6_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nssv3008596 | Remapped | Perfect | NC_000017.11:g.(?_ 65218252)_(6537621 6_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nssv3008887 | Remapped | Perfect | NC_000017.11:g.(?_ 65218252)_(6537621 6_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nssv3009564 | Remapped | Perfect | NC_000017.11:g.(?_ 65218252)_(6537621 6_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nssv3009813 | Remapped | Perfect | NC_000017.11:g.(?_ 65218252)_(6537621 6_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nssv3010233 | Remapped | Perfect | NC_000017.11:g.(?_ 65218252)_(6537621 6_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,218,252 | 65,376,216 |
| nssv3006533 | Remapped | Perfect | NC_000017.10:g.(?_ 63214370)_(6337233 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nssv3006814 | Remapped | Perfect | NC_000017.10:g.(?_ 63214370)_(6337233 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nssv3008596 | Remapped | Perfect | NC_000017.10:g.(?_ 63214370)_(6337233 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nssv3008887 | Remapped | Perfect | NC_000017.10:g.(?_ 63214370)_(6337233 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nssv3009564 | Remapped | Perfect | NC_000017.10:g.(?_ 63214370)_(6337233 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nssv3009813 | Remapped | Perfect | NC_000017.10:g.(?_ 63214370)_(6337233 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nssv3010233 | Remapped | Perfect | NC_000017.10:g.(?_ 63214370)_(6337233 4_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,214,370 | 63,372,334 |
| nssv3006533 | Submitted genomic | NC_000017.8:g.(?_6 3764471)_(63922435 _?)del | NCBI34 (hg16) | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 | ||
| nssv3006814 | Submitted genomic | NC_000017.8:g.(?_6 3764471)_(63922435 _?)del | NCBI34 (hg16) | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 | ||
| nssv3008596 | Submitted genomic | NC_000017.8:g.(?_6 3764471)_(63922435 _?)del | NCBI34 (hg16) | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 | ||
| nssv3008887 | Submitted genomic | NC_000017.8:g.(?_6 3764471)_(63922435 _?)del | NCBI34 (hg16) | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 | ||
| nssv3009564 | Submitted genomic | NC_000017.8:g.(?_6 3764471)_(63922435 _?)del | NCBI34 (hg16) | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 | ||
| nssv3009813 | Submitted genomic | NC_000017.8:g.(?_6 3764471)_(63922435 _?)del | NCBI34 (hg16) | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 | ||
| nssv3010233 | Submitted genomic | NC_000017.8:g.(?_6 3764471)_(63922435 _?)del | NCBI34 (hg16) | NC_000017.8 | Chr17 | 63,764,471 | 63,922,435 |