nsv477914
- 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:6
- 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: 213 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 213 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 109 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv477914 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 148,403,075 | 148,403,080 |
| nsv477914 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 148,100,167 | 148,100,172 |
| nsv477914 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 147,731,100 | 147,731,105 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3020071 | complex substitution | SAMN00001588 | Sequencing | Sequence alignment | 1,045 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3020071 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 148,403,075 | 148,403,080 |
| nssv3020071 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 148,100,167 | 148,100,172 |
| nssv3020071 | Submitted genomic | NCBI36 (hg18) | NC_000007.12 | Chr7 | 147,731,100 | 147,731,105 |