esv1003020
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,802
- Publication(s):Pang et al. 2010
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: 175 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 175 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 69 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1003020 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 21,864,040 | 21,885,841 |
| esv1003020 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 22,190,533 | 22,212,334 |
| esv1003020 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 22,063,120 | 22,084,921 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564134 | Remapped | Perfect | NC_000001.11:g.(21 864040_?)_(?_21885 841)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 21,864,040 | 21,885,841 |
| essv3564134 | Remapped | Perfect | NC_000001.10:g.(22 190533_?)_(?_22212 334)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 22,190,533 | 22,212,334 |
| essv3564134 | Submitted genomic | NC_000001.9:g.(220 63120_?)_(?_220849 21)del9822 | NCBI36 (hg18) | NC_000001.9 | Chr1 | 22,063,120 | 22,084,921 |