nsv473590
- Organism: Homo sapiens
- Study:nstd35 (Kidd et al. 2010)
- Variant Type:complex substitution
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3
- Description:complex allele - no allele length provided
- Publication(s):Kidd 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: 120 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 36 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv473590 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 94,363,765 | 94,363,767 |
| nsv473590 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 94,830,102 | 94,830,104 |
| nsv473590 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 93,899,855 | 93,899,857 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3020121 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 94,363,765 | 94,363,767 |
| nssv3020121 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 94,830,102 | 94,830,104 |
| nssv3020121 | Submitted genomic | NCBI36 (hg18) | NC_000014.7 | Chr14 | 93,899,855 | 93,899,857 |