esv2643528
- 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:2,186
- 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: 255 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 255 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 163 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2643528 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 168,692,930 | 168,692,930 | 168,695,115 | 168,695,115 |
| esv2643528 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 169,093,044 | 169,093,571 | 169,094,718 | 169,095,229 |
| esv2643528 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 168,834,969 | 168,835,496 | 168,836,643 | 168,837,154 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5188374 | Remapped | Perfect | NC_000006.12:g.(16 8692930_168692930) _(168695115_168695 115)inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 168,692,930 | 168,692,930 | 168,695,115 | 168,695,115 |
| essv5188374 | Remapped | Perfect | NC_000006.11:g.(16 9093044_169093571) _(169094718_169095 229)inv | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 169,093,044 | 169,093,571 | 169,094,718 | 169,095,229 |
| essv5188374 | Submitted genomic | NC_000006.10:g.(16 8834969_168835496) _(168836643_168837 154)inv | NCBI36 (hg18) | NC_000006.10 | Chr6 | 168,834,969 | 168,835,496 | 168,836,643 | 168,837,154 |