nsv474483
- 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:9
- 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: 247 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 248 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 112 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv474483 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 84,345,473 | 84,345,481 |
| nsv474483 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 84,919,608 | 84,919,616 |
| nsv474483 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 83,817,609 | 83,817,617 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3017317 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 84,345,473 | 84,345,481 |
| nssv3017317 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 84,919,608 | 84,919,616 |
| nssv3017317 | Submitted genomic | NCBI36 (hg18) | NC_000013.9 | Chr13 | 83,817,609 | 83,817,617 |