esv1819974
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:182,202
- Publication(s):Pinto et al. 2011
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: 590 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 590 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1819974 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 135,190,743 | 135,372,944 |
| esv1819974 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 136,111,898 | 136,294,099 |
| esv1819974 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 136,331,348 | 136,513,549 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4367938 | Remapped | Perfect | NC_000004.12:g.(?_ 135190743)_(135372 944_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 135,190,743 | 135,372,944 |
| essv4367938 | Remapped | Perfect | NC_000004.11:g.(?_ 136111898)_(136294 099_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 136,111,898 | 136,294,099 |
| essv4367938 | Submitted genomic | NC_000004.10:g.(?_ 136331348)_(136513 549_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 136,331,348 | 136,513,549 |