esv2609145
- 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:36,658
- 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: 2284 SVs from 99 studies. See in: genome view
Overlapping variant regions from other studies: 1863 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1120 SVs from 32 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2609145 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 46,489,859 | 46,489,859 | 46,526,516 | 46,526,516 |
| esv2609145 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 47,023,101 | 47,023,140 | 47,059,577 | 47,059,579 |
| esv2609145 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 46,443,107 | 46,443,146 | 46,479,583 | 46,479,585 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5178220 | Remapped | Good | NC_000010.11:g.(46 489859_46489859)_( 46526516_46526516) inv | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 46,489,859 | 46,489,859 | 46,526,516 | 46,526,516 |
| essv5178220 | Remapped | Perfect | NC_000010.10:g.(47 023101_47023140)_( 47059577_47059579) inv | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 47,023,101 | 47,023,140 | 47,059,577 | 47,059,579 |
| essv5178220 | Submitted genomic | NC_000010.9:g.(464 43107_46443146)_(4 6479583_46479585)i nv | NCBI36 (hg18) | NC_000010.9 | Chr10 | 46,443,107 | 46,443,146 | 46,479,583 | 46,479,585 |