esv3666953
- 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:83
- 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: 160 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 160 SVs from 39 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3666953 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 159,078,086 | 159,078,168 |
| esv3666953 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 158,795,875 | 158,795,957 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16489461 | inversion | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16489461 | Remapped | Perfect | NC_000003.12:g.159 078086_159078168in v82 | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 159,078,086 | 159,078,168 |
| essv16489461 | Submitted genomic | NC_000003.11:g.158 795875_158795957in v82 | GRCh37 (hg19) | NC_000003.11 | Chr3 | 158,795,875 | 158,795,957 |