esv992100
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,405
- 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: 368 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 368 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 171 SVs from 20 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv992100 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 165,158,182 | 165,171,586 |
| esv992100 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 166,014,692 | 166,028,096 |
| esv992100 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 165,722,938 | 165,736,342 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586381 | Remapped | Perfect | NC_000002.12:g.(?_ 165158182)_(165171 586_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 165,158,182 | 165,171,586 |
| essv3586381 | Remapped | Perfect | NC_000002.11:g.(?_ 166014692)_(166028 096_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 166,014,692 | 166,028,096 |
| essv3586381 | Submitted genomic | NC_000002.10:g.(?_ 165722938)_(165736 342_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 165,722,938 | 165,736,342 |