esv2469970
- 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:56,438
- 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: 759 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 759 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 211 SVs from 23 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
esv2469970 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 131,346,434 | 131,347,153 | 131,402,614 | 131,402,871 |
esv2469970 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 131,830,979 | 131,831,698 | 131,887,159 | 131,887,416 |
esv2469970 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 130,396,932 | 130,397,651 | 130,453,112 | 130,453,369 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
essv5386904 | Remapped | Perfect | NC_000012.12:g.(13 1346434_131347153) _(131402614_131402 871)inv | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 131,346,434 | 131,347,153 | 131,402,614 | 131,402,871 |
essv5386904 | Remapped | Perfect | NC_000012.11:g.(13 1830979_131831698) _(131887159_131887 416)inv | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 131,830,979 | 131,831,698 | 131,887,159 | 131,887,416 |
essv5386904 | Submitted genomic | NC_000012.10:g.(13 0396932_130397651) _(130453112_130453 369)inv | NCBI36 (hg18) | NC_000012.10 | Chr12 | 130,396,932 | 130,397,651 | 130,453,112 | 130,453,369 |