esv1007842
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:17,405
- Publication(s):Pang et al. 2010
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: 350 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 350 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 83 SVs from 18 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1007842 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 100,989,319 | 101,006,723 |
| esv1007842 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 100,632,600 | 100,650,004 |
| esv1007842 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 100,419,320 | 100,436,724 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563479 | Remapped | Perfect | NC_000007.14:g.(10 0989319_?)_(?_1010 06723)ins16814 | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 100,989,319 | 101,006,723 |
| essv3563479 | Remapped | Perfect | NC_000007.13:g.(10 0632600_?)_(?_1006 50004)ins16814 | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 100,632,600 | 100,650,004 |
| essv3563479 | Submitted genomic | NC_000007.12:g.(10 0419320_?)_(?_1004 36724)ins16814 | NCBI36 (hg18) | NC_000007.12 | Chr7 | 100,419,320 | 100,436,724 |