nsv482747
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:14
- Validation:Not tested
- Clinical Assertions: No
- Region Size:149,437
- 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: 525 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 525 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482747 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nsv482747 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nsv482747 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3005878 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3006272 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3006758 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3007163 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3007787 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3008147 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3008878 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3009067 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3009344 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3010056 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3010126 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3010268 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3010341 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv3010428 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3005878 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3006272 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3006758 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3007163 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3007787 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3008147 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3008878 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3009067 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3009344 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3010056 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3010126 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3010268 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3010341 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3010428 | Remapped | Perfect | NC_000004.12:g.(?_ 123553131)_(123702 567_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 123,553,131 | 123,702,567 |
| nssv3005878 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3006272 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3006758 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3007163 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3007787 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3008147 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3008878 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3009067 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3009344 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3010056 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3010126 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3010268 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3010341 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3010428 | Remapped | Perfect | NC_000004.11:g.(?_ 124474286)_(124623 722_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 124,474,286 | 124,623,722 |
| nssv3005878 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3006272 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3006758 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3007163 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3007787 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3008147 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3008878 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3009067 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3009344 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3010056 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3010126 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3010268 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3010341 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 | ||
| nssv3010428 | Submitted genomic | NC_000004.8:g.(?_1 24933107)_(1250825 43_?)del | NCBI34 (hg16) | NC_000004.8 | Chr4 | 124,933,107 | 125,082,543 |