nsv823144
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:40,298
- Publication(s):Park et al. 2010
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: 192 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 192 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 72 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv823144 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 94,836,532 | 94,876,829 |
| nsv823144 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 94,172,237 | 94,212,534 |
| nsv823144 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 94,197,993 | 94,238,290 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1438823 | Remapped | Perfect | NC_000005.10:g.(?_ 94836532)_(9487682 9_?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 94,836,532 | 94,876,829 |
| nssv1438823 | Remapped | Perfect | NC_000005.9:g.(?_9 4172237)_(94212534 _?)del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 94,172,237 | 94,212,534 |
| nssv1438823 | Submitted genomic | NC_000005.8:g.(?_9 4197993)_(94238290 _?)del | NCBI36 (hg18) | NC_000005.8 | Chr5 | 94,197,993 | 94,238,290 |