esv4584
- Organism: Homo sapiens
- Study:estd3 (Wang et al. 2008)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,173
- 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: 278 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 278 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 181 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv4584 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 18,425,681 | 18,427,853 |
| esv4584 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 19,797,998 | 19,800,170 |
| esv4584 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000021.7 | Chr21 | 18,719,869 | 18,722,041 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv27025 | inversion | YH | Sequencing | Read depth and paired-end mapping | 2,682 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv27025 | Remapped | Perfect | NC_000021.9:g.(184 25681_?)_(?_184278 53)inv | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 18,425,681 | 18,427,853 |
| essv27025 | Remapped | Perfect | NC_000021.8:g.(197 97998_?)_(?_198001 70)inv | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 19,797,998 | 19,800,170 |
| essv27025 | Submitted genomic | NC_000021.7:g.(187 19869_?)_(?_187220 41)inv | NCBI36 (hg18) | NC_000021.7 | Chr21 | 18,719,869 | 18,722,041 |