nsv930458
- Organism: Homo sapiens
- Study:nstd76 (Watson et al. 2013)
- Variant Type:complex substitution
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:37,678
- Publication(s):Watson et al. 2013
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: 2514 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 2147 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 2409 SVs from 86 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv930458 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 106,075,078 | 106,112,755 |
| nsv930458 | Remapped | Good | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187600.1 | Chr14|NT_1 87600.1 | 542,847 | 580,524 |
| nsv930458 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 106,531,320 | 106,569,343 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1607653 | complex substitution | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|
| nssv1607653 | Remapped | Good | GRCh38.p12 | Second Pass | NT_187600.1 | Chr14|NT_1 87600.1 | 542,847 | 580,524 |
| nssv1607653 | Remapped | Good | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 106,075,078 | 106,112,755 |
| nssv1607653 | Submitted genomic | GRCh37 (hg19) | NC_000014.8 | Chr14 | 106,531,320 | 106,569,343 |