esv3666934
- 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:84
- 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: 196 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 202 SVs from 48 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3666934 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 207,119,002 | 207,119,085 |
| esv3666934 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 207,292,347 | 207,292,430 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16489444 | inversion | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16489444 | Remapped | Perfect | NC_000001.11:g.207 119002_207119085in v83 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 207,119,002 | 207,119,085 |
| essv16489444 | Submitted genomic | NC_000001.10:g.207 292347_207292430in v83 | GRCh37 (hg19) | NC_000001.10 | Chr1 | 207,292,347 | 207,292,430 |