esv1782250
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- 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):Levy et al. 2007
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: 83 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 83 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 22 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1782250 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 111,365,760 | 111,365,761 |
| esv1782250 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 111,803,564 | 111,803,565 |
| esv1782250 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 110,287,947 | 110,287,948 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3902617 | Remapped | Perfect | NC_000012.12:g.111 365760_111365761de l | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 111,365,760 | 111,365,761 |
| essv3902617 | Remapped | Perfect | NC_000012.11:g.111 803564_111803565de l | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 111,803,564 | 111,803,565 |
| essv3902617 | Submitted genomic | NC_000012.10:g.110 287947_110287948de l | NCBI36 (hg18) | NC_000012.10 | Chr12 | 110,287,947 | 110,287,948 |