esv2439266
- 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:2,150
- 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: 165 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 165 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 48 SVs from 15 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
esv2439266 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 13,062,087 | 13,062,995 | 13,063,274 | 13,064,236 |
esv2439266 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 13,104,087 | 13,104,995 | 13,105,274 | 13,106,236 |
esv2439266 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 13,144,093 | 13,145,001 | 13,145,280 | 13,146,242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
essv5192548 | Remapped | Perfect | NC_000010.11:g.(13 062087_13062995)_( 13063274_13064236) inv | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 13,062,087 | 13,062,995 | 13,063,274 | 13,064,236 |
essv5192548 | Remapped | Perfect | NC_000010.10:g.(13 104087_13104995)_( 13105274_13106236) inv | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 13,104,087 | 13,104,995 | 13,105,274 | 13,106,236 |
essv5192548 | Submitted genomic | NC_000010.9:g.(131 44093_13145001)_(1 3145280_13146242)i nv | NCBI36 (hg18) | NC_000010.9 | Chr10 | 13,144,093 | 13,145,001 | 13,145,280 | 13,146,242 |