esv1209927
- 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:6
- 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: 221 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 221 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 100 SVs from 14 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1209927 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 19,971,245 | 19,971,250 |
| esv1209927 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 20,545,385 | 20,545,390 |
| esv1209927 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 19,443,385 | 19,443,390 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4327821 | Remapped | Perfect | NC_000013.11:g.199 71245_19971250del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 19,971,245 | 19,971,250 |
| essv4327821 | Remapped | Perfect | NC_000013.10:g.205 45385_20545390del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 20,545,385 | 20,545,390 |
| essv4327821 | Submitted genomic | NC_000013.9:g.1944 3385_19443390del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 19,443,385 | 19,443,390 |