nsv834033
- Organism: Homo sapiens
- Study:nstd68 (Wong et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:11
- Validation:Not tested
- Clinical Assertions: No
- Region Size:133,552
- 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: 1112 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1112 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 58 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv834033 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nsv834033 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nsv834033 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1455329 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455330 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455331 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455332 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455333 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455334 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455335 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455336 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455337 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455338 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1455339 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1455329 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455330 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455331 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455332 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455333 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455334 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455335 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455336 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455337 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455338 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455339 | Remapped | Perfect | NC_000020.11:g.(63 421436_?)_(?_63554 987)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 63,421,436 | 63,554,987 |
| nssv1455329 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455330 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455331 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455332 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455333 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455334 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455335 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455336 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455337 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455338 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455339 | Remapped | Perfect | NC_000020.10:g.(62 052789_?)_(?_62186 340)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 62,052,789 | 62,186,340 |
| nssv1455329 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455330 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455331 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455332 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455333 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455334 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455335 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455336 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455337 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455338 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 | ||
| nssv1455339 | Submitted genomic | NC_000020.9:g.(615 23233_?)_(?_616567 84)dup | NCBI35 (hg17) | NC_000020.9 | Chr20 | 61,523,233 | 61,656,784 |