esv2427673
- 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:20,580
- 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: 464 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 464 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 201 SVs from 13 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2427673 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 46,951,230 | 46,951,230 | 46,971,809 | 46,971,809 |
| esv2427673 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 46,810,665 | 46,810,994 | 46,830,499 | 46,831,200 |
| esv2427673 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 46,695,609 | 46,695,938 | 46,715,443 | 46,716,144 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5181113 | Remapped | Good | NC_000023.11:g.(46 951230_46951230)_( 46971809_46971809) inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 46,951,230 | 46,951,230 | 46,971,809 | 46,971,809 |
| essv5181113 | Remapped | Perfect | NC_000023.10:g.(46 810665_46810994)_( 46830499_46831200) inv | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 46,810,665 | 46,810,994 | 46,830,499 | 46,831,200 |
| essv5181113 | Submitted genomic | NC_000023.9:g.(466 95609_46695938)_(4 6715443_46716144)i nv | NCBI36 (hg18) | NC_000023.9 | ChrX | 46,695,609 | 46,695,938 | 46,715,443 | 46,716,144 |