nsv821600
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,668
- Publication(s):Ju 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: 507 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 510 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 12 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821600 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 140,999,599 | 141,013,266 |
| nsv821600 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 140,084,056 | 140,107,442 |
| nsv821600 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 139,909,430 | 139,935,108 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420210 | Remapped | Pass | NC_000023.11:g.(?_ 140999599)_(141013 266_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 140,999,599 | 141,013,266 |
| nssv1420210 | Remapped | Pass | NC_000023.10:g.(?_ 140084056)_(140107 442_?)del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 140,084,056 | 140,107,442 |
| nssv1420210 | Submitted genomic | NC_000023.9:g.(?_1 39909430)_(1399351 08_?)del | NCBI36 (hg18) | NC_000023.9 | ChrX | 139,909,430 | 139,935,108 |