esv2316888
- Organism: Homo sapiens
- Study:estd194 (Bentley et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2
- Publication(s):Bentley 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: 123 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 35 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2316888 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 112,092,257 | 112,092,258 |
| esv2316888 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 111,962,981 | 111,962,982 |
| esv2316888 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 111,468,191 | 111,468,192 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4817314 | Remapped | Perfect | NC_000011.10:g.112 092257_112092258de lA | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 112,092,257 | 112,092,258 |
| essv4817314 | Remapped | Perfect | NC_000011.9:g.1119 62981_111962982del A | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 111,962,981 | 111,962,982 |
| essv4817314 | Submitted genomic | NC_000011.8:g.1114 68191_111468192del A | NCBI36 (hg18) | NC_000011.8 | Chr11 | 111,468,191 | 111,468,192 |