nsv499513
- Organism: Homo sapiens
- Study:nstd47 (Kidd et al. 2010b)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:11,195
- 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: 571 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 571 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 304 SVs from 24 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv499513 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 1,237,915 | 1,249,109 |
| nsv499513 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 1,287,916 | 1,299,110 |
| nsv499513 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 1,227,917 | 1,239,111 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv585512 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv585512 | Remapped | Perfect | NC_000016.10:g.123 7915_1249109inv | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 1,237,915 | 1,249,109 |
| nssv585512 | Remapped | Perfect | NC_000016.9:g.1287 916_1299110inv | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 1,287,916 | 1,299,110 |
| nssv585512 | Submitted genomic | NC_000016.8:g.1227 917_1239111inv | NCBI36 (hg18) | NC_000016.8 | Chr16 | 1,227,917 | 1,239,111 |