nsv821337
- 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:70,768
- 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: 2627 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 2627 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1282 SVs from 32 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821337 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 78,257,044 | 78,327,811 |
| nsv821337 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 78,966,761 | 79,037,528 |
| nsv821337 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 79,023,480 | 79,094,247 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420595 | Remapped | Perfect | NC_000006.12:g.(?_ 78257044)_(7832781 1_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 78,257,044 | 78,327,811 |
| nssv1420595 | Remapped | Perfect | NC_000006.11:g.(?_ 78966761)_(7903752 8_?)del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 78,966,761 | 79,037,528 |
| nssv1420595 | Submitted genomic | NC_000006.10:g.(?_ 79023480)_(7909424 7_?)del | NCBI36 (hg18) | NC_000006.10 | Chr6 | 79,023,480 | 79,094,247 |