esv1005511
- 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:24,977
- 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: 468 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 468 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 176 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1005511 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 73,941,104 | 73,966,080 |
| esv1005511 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 73,160,939 | 73,185,915 |
| esv1005511 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 73,077,664 | 73,102,640 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563471 | Remapped | Perfect | NC_000023.11:g.(73 941104_?)_(?_73966 080)ins11795 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 73,941,104 | 73,966,080 |
| essv3563471 | Remapped | Perfect | NC_000023.10:g.(73 160939_?)_(?_73185 915)ins11795 | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 73,160,939 | 73,185,915 |
| essv3563471 | Submitted genomic | NC_000023.9:g.(730 77664_?)_(?_731026 40)ins11795 | NCBI36 (hg18) | NC_000023.9 | ChrX | 73,077,664 | 73,102,640 |