esv1405784
- 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:2
- 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: 114 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 118 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 26 SVs from 9 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1405784 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 160,638,165 | 160,638,166 |
| esv1405784 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 160,607,955 | 160,607,956 |
| esv1405784 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 158,874,579 | 158,874,580 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3696486 | Remapped | Perfect | NC_000001.11:g.160 638165_160638166de l | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 160,638,165 | 160,638,166 |
| essv3696486 | Remapped | Perfect | NC_000001.10:g.160 607955_160607956de l | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 160,607,955 | 160,607,956 |
| essv3696486 | Submitted genomic | NC_000001.9:g.1588 74579_158874580del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 158,874,579 | 158,874,580 |