esv1189933
- 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:5,834
- 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: 317 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 317 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 25 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1189933 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 32,060,560 | 32,066,393 |
| esv1189933 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 32,102,052 | 32,107,885 |
| esv1189933 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 32,077,056 | 32,082,889 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3998228 | Remapped | Perfect | NC_000003.12:g.320 60560_32066393del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 32,060,560 | 32,066,393 |
| essv3998228 | Remapped | Perfect | NC_000003.11:g.321 02052_32107885del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 32,102,052 | 32,107,885 |
| essv3998228 | Submitted genomic | NC_000003.10:g.320 77056_32082889del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 32,077,056 | 32,082,889 |