nsv818088
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:104,088
- Publication(s):Wang et al. 2007
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: 460 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 460 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 42 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv818088 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 152,828,417 | 152,932,504 |
| nsv818088 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 153,684,931 | 153,789,018 |
| nsv818088 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000002.9 | Chr2 | 153,510,439 | 153,614,526 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1417317 | Remapped | Perfect | NC_000002.12:g.(?_ 152828417)_(152932 504_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 152,828,417 | 152,932,504 |
| nssv1417317 | Remapped | Perfect | NC_000002.11:g.(?_ 153684931)_(153789 018_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 153,684,931 | 153,789,018 |
| nssv1417317 | Submitted genomic | NC_000002.9:g.(?_1 53510439)_(1536145 26_?)del | NCBI35 (hg17) | NC_000002.9 | Chr2 | 153,510,439 | 153,614,526 |