esv1720905
- 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:51
- 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: 123 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 120 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 22 SVs from 12 studies. See in: genome view
Overlapping variant regions from other studies: 55 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1720905 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 57,745,345 | 57,745,395 |
| esv1720905 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000016.9 | Chr16 | 57,779,257 | 57,779,307 |
| esv1720905 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871085.1 | Chr16|NW_0 03871085.1 | 5,236 | 5,286 |
| esv1720905 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 56,336,758 | 56,336,808 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4134507 | Remapped | Perfect | NC_000016.10:g.577 45345_57745395del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 57,745,345 | 57,745,395 |
| essv4134507 | Remapped | Perfect | NW_003871085.1:g.5 236_5286del | GRCh37.p13 | First Pass | NW_003871085.1 | Chr16|NW_0 03871085.1 | 5,236 | 5,286 |
| essv4134507 | Remapped | Perfect | NC_000016.9:g.5777 9257_57779307del | GRCh37.p13 | Second Pass | NC_000016.9 | Chr16 | 57,779,257 | 57,779,307 |
| essv4134507 | Submitted genomic | NC_000016.8:g.5633 6758_56336808del | NCBI36 (hg18) | NC_000016.8 | Chr16 | 56,336,758 | 56,336,808 |