esv29975
- 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:27,936
- 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: 236 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 63 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29975 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 9,337,250 | 9,365,185 |
| esv29975 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 9,240,567 | 9,268,502 |
| esv29975 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 9,181,292 | 9,209,227 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84214 | Remapped | Perfect | NC_000017.11:g.(?_ 9337250)_(9365185_ ?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 9,337,250 | 9,365,185 |
| essv84214 | Remapped | Perfect | NC_000017.10:g.(?_ 9240567)_(9268502_ ?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 9,240,567 | 9,268,502 |
| essv84214 | Submitted genomic | NC_000017.9:g.(?_9 181292)_(9209227_? )del | NCBI36 (hg18) | NC_000017.9 | Chr17 | 9,181,292 | 9,209,227 |