esv1791683
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Levy et al. 2007
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: 145 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 145 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 49 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791683 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 146,495,809 | 146,495,809 |
| esv1791683 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 147,416,961 | 147,416,961 |
| esv1791683 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 147,636,411 | 147,636,411 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3757656 | Remapped | Perfect | NC_000004.12:g.146 495809_146495810in sCA | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 146,495,809 | 146,495,809 |
| essv3757656 | Remapped | Perfect | NC_000004.11:g.147 416961_147416962in sCA | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 147,416,961 | 147,416,961 |
| essv3757656 | Submitted genomic | NC_000004.10:g.147 636411_147636412in sCA | NCBI36 (hg18) | NC_000004.10 | Chr4 | 147,636,411 | 147,636,411 |