esv1000400
- 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:16,092
- 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: 480 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 479 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 186 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1000400 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 56,768,208 | 56,784,299 |
| esv1000400 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 56,794,641 | 56,810,732 |
| esv1000400 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 56,811,366 | 56,827,457 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563718 | Remapped | Perfect | NC_000023.11:g.(56 768208_?)_(?_56784 299)ins12923 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 56,768,208 | 56,784,299 |
| essv3563718 | Remapped | Perfect | NC_000023.10:g.(56 794641_?)_(?_56810 732)ins12923 | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 56,794,641 | 56,810,732 |
| essv3563718 | Submitted genomic | NC_000023.9:g.(568 11366_?)_(?_568274 57)ins12923 | NCBI36 (hg18) | NC_000023.9 | ChrX | 56,811,366 | 56,827,457 |