esv1914952
- Organism: Homo sapiens
- Study:estd193 (Feuk et al. 2005)
- Variant Type:inversion
- Method Type:PCR
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,065
- Publication(s):Feuk et al. 2005
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: 276 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 276 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 3 SVs from 1 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv1914952 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 85,155,131 | 85,156,195 |
esv1914952 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 85,188,737 | 85,189,801 |
esv1914952 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000016.8 | Chr16 | 83,746,238 | 83,747,302 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
essv4491059 | inversion | PCR | Manual observation |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv4491059 | Remapped | Perfect | NC_000016.10:g.851 55131_85156195inv | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 85,155,131 | 85,156,195 |
essv4491059 | Remapped | Perfect | NC_000016.9:g.8518 8737_85189801inv | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 85,188,737 | 85,189,801 |
essv4491059 | Submitted genomic | NC_000016.8:g.8374 6238_83747302inv | NCBI35 (hg17) | NC_000016.8 | Chr16 | 83,746,238 | 83,747,302 |