nsv831987
- Organism: Homo sapiens
- Study:nstd68 (Wong et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:14
- Validation:Not tested
- Clinical Assertions: No
- Region Size:220,940
- 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: 560 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 560 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 31 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv831987 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nsv831987 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nsv831987 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1448733 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1448734 | copy number gain | BAC aCGH | Probe signal intensity |
| nssv1448735 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448736 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448737 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448738 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448741 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448742 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448743 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448744 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448745 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448746 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448747 | copy number loss | BAC aCGH | Probe signal intensity |
| nssv1448748 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1448733 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448734 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448735 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448736 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448737 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448738 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448741 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448742 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448743 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448744 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448745 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448746 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448747 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448748 | Remapped | Perfect | NC_000010.11:g.(11 1670749_?)_(?_1118 91688)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 111,670,749 | 111,891,688 |
| nssv1448733 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448734 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448735 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448736 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448737 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448738 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448741 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448742 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448743 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448744 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448745 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448746 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448747 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448748 | Remapped | Perfect | NC_000010.10:g.(11 3430507_?)_(?_1136 51446)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 113,430,507 | 113,651,446 |
| nssv1448733 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448734 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448735 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448736 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448737 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448738 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448741 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448742 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448743 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448744 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448745 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448746 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448747 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 | ||
| nssv1448748 | Submitted genomic | NC_000010.8:g.(113 420497_?)_(?_11364 1436)del | NCBI35 (hg17) | NC_000010.8 | Chr10 | 113,420,497 | 113,641,436 |