esv2757332
- Organism: Homo sapiens
- Study:estd1 (Redon et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:134,109
- Publication(s):Redon 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: 733 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 739 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 43 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2757332 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 30,255,387 | 30,389,495 |
| esv2757332 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 30,255,385 | 30,389,493 |
| esv2757332 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000009.9 | Chr9 | 30,245,385 | 30,379,493 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv9491 | Remapped | Perfect | NC_000009.12:g.(30 255387_30265838)_( 30351288_30389495) dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 30,255,387 | 30,265,838 | 30,351,288 | 30,389,495 |
| essv12427 | Remapped | Perfect | NC_000009.12:g.(30 255387_30255387)_( 30375988_30389495) dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 30,255,387 | 30,255,387 | 30,375,988 | 30,389,495 |
| essv9491 | Remapped | Perfect | NC_000009.11:g.(30 255385_30265836)_( 30351286_30389493) dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 30,255,385 | 30,265,836 | 30,351,286 | 30,389,493 |
| essv12427 | Remapped | Perfect | NC_000009.11:g.(30 255385_30255385)_( 30375986_30389493) dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 30,255,385 | 30,255,385 | 30,375,986 | 30,389,493 |
| essv9491 | Submitted genomic | NC_000009.9:g.(302 45385_30255836)_(3 0341286_30379493)d up | NCBI35 (hg17) | NC_000009.9 | Chr9 | 30,245,385 | 30,255,836 | 30,341,286 | 30,379,493 | ||
| essv12427 | Submitted genomic | NC_000009.9:g.(302 45385_30245385)_(3 0365986_30379493)d up | NCBI35 (hg17) | NC_000009.9 | Chr9 | 30,245,385 | 30,245,385 | 30,365,986 | 30,379,493 |