esv29973
- 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:63,967
- 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: 691 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 691 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 328 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29973 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 136,795,692 | 136,859,658 |
| esv29973 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 139,690,144 | 139,754,110 |
| esv29973 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 138,809,965 | 138,873,931 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84212 | Remapped | Perfect | NC_000009.12:g.(?_ 136795692)_(136859 658_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 136,795,692 | 136,859,658 |
| essv84212 | Remapped | Perfect | NC_000009.11:g.(?_ 139690144)_(139754 110_?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 139,690,144 | 139,754,110 |
| essv84212 | Submitted genomic | NC_000009.10:g.(?_ 138809965)_(138873 931_?)del | NCBI36 (hg18) | NC_000009.10 | Chr9 | 138,809,965 | 138,873,931 |