esv5169
- Organism: Homo sapiens
- Study:estd3 (Wang et al. 2008)
- Variant Type:sequence alteration
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:355
- Publication(s):Wang et al. 2008
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: 274 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 274 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 140 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv5169 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 2,514,808 | 2,515,162 |
| esv5169 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 2,554,442 | 2,554,796 |
| esv5169 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 2,520,968 | 2,521,322 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv27610 | sequence alteration | YH | Sequencing | Read depth and paired-end mapping | 2,682 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|
| essv27610 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 2,514,808 | 2,515,162 |
| essv27610 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 2,554,442 | 2,554,796 |
| essv27610 | Submitted genomic | NCBI36 (hg18) | NC_000007.12 | Chr7 | 2,520,968 | 2,521,322 |