esv1350123
- 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: 99 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 29 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1350123 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 32,403,200 | 32,403,201 |
| esv1350123 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 32,442,812 | 32,442,813 |
| esv1350123 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 32,409,337 | 32,409,338 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4367655 | Remapped | Perfect | NC_000007.14:g.324 03200_32403201del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 32,403,200 | 32,403,201 |
| essv4367655 | Remapped | Perfect | NC_000007.13:g.324 42812_32442813del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 32,442,812 | 32,442,813 |
| essv4367655 | Submitted genomic | NC_000007.12:g.324 09337_32409338del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 32,409,337 | 32,409,338 |