esv29967
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:106,634
- 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: 593 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 593 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 240 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29967 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 52,285,116 | 52,391,749 |
| esv29967 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 52,678,900 | 52,785,533 |
| esv29967 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 50,965,167 | 51,071,800 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84206 | Remapped | Perfect | NC_000012.12:g.(?_ 52285116)_(5239174 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 52,285,116 | 52,391,749 |
| essv84206 | Remapped | Perfect | NC_000012.11:g.(?_ 52678900)_(5278553 3_?)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 52,678,900 | 52,785,533 |
| essv84206 | Submitted genomic | NC_000012.10:g.(?_ 50965167)_(5107180 0_?)dup | NCBI36 (hg18) | NC_000012.10 | Chr12 | 50,965,167 | 51,071,800 |