esv2422262
- Organism: Homo sapiens
- Study:estd196 (Simon-Sanchez et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:131,376
- Publication(s):Simon-Sanchez et al. 2006
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: 341 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 341 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 20 SVs from 2 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2422262 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 95,795,772 | 95,927,147 |
| esv2422262 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 96,261,328 | 96,392,703 |
| esv2422262 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 95,973,349 | 96,104,724 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5161551 | Remapped | Perfect | NC_000001.11:g.(?_ 95795772)_(9592714 7_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 95,795,772 | 95,927,147 |
| essv5161551 | Remapped | Perfect | NC_000001.10:g.(?_ 96261328)_(9639270 3_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 96,261,328 | 96,392,703 |
| essv5161551 | Submitted genomic | NC_000001.8:g.(?_9 5973349)_(96104724 _?)dup | NCBI35 (hg17) | NC_000001.8 | Chr1 | 95,973,349 | 96,104,724 |