esv2604561
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,567
- Description:originalFile=Yoruban_inv.gff
- Publication(s):McKernan et al. 2009
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: 130 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 129 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 29 SVs from 16 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2604561 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 71,569,794 | 71,570,082 | 71,578,564 | 71,579,360 |
| esv2604561 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 71,280,840 | 71,281,128 | 71,289,610 | 71,290,406 |
| esv2604561 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 70,958,488 | 70,958,776 | 70,967,258 | 70,968,054 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5334680 | Remapped | Perfect | NC_000011.10:g.(71 569794_71570082)_( 71578564_71579360) inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 71,569,794 | 71,570,082 | 71,578,564 | 71,579,360 |
| essv5334680 | Remapped | Perfect | NC_000011.9:g.(712 80840_71281128)_(7 1289610_71290406)i nv | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 71,280,840 | 71,281,128 | 71,289,610 | 71,290,406 |
| essv5334680 | Submitted genomic | NC_000011.8:g.(709 58488_70958776)_(7 0967258_70968054)i nv | NCBI36 (hg18) | NC_000011.8 | Chr11 | 70,958,488 | 70,958,776 | 70,967,258 | 70,968,054 |