esv3666949
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:102
- Publication(s):Besenbacher et al. 2015
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: 544 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 528 SVs from 30 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3666949 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 155,093,524 | 155,093,625 |
| esv3666949 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 154,321,799 | 154,321,900 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16489458 | inversion | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16489458 | Remapped | Perfect | NC_000023.11:g.155 093524_155093625in v101 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 155,093,524 | 155,093,625 |
| essv16489458 | Submitted genomic | NC_000023.10:g.154 321799_154321900in v101 | GRCh37 (hg19) | NC_000023.10 | ChrX | 154,321,799 | 154,321,900 |