esv2423930
- 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:1,935
- 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: 209 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 209 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 62 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv2423930 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 194,668,372 | 194,669,488 | 194,669,566 | 194,670,306 |
| esv2423930 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 194,637,502 | 194,638,618 | 194,638,696 | 194,639,436 |
| esv2423930 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 192,904,125 | 192,905,241 | 192,905,319 | 192,906,059 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv5394106 | Remapped | Perfect | NC_000001.11:g.(19 4668372_194669488) _(194669566_194670 306)inv | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 194,668,372 | 194,669,488 | 194,669,566 | 194,670,306 |
| essv5394106 | Remapped | Perfect | NC_000001.10:g.(19 4637502_194638618) _(194638696_194639 436)inv | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 194,637,502 | 194,638,618 | 194,638,696 | 194,639,436 |
| essv5394106 | Submitted genomic | NC_000001.9:g.(192 904125_192905241)_ (192905319_1929060 59)inv | NCBI36 (hg18) | NC_000001.9 | Chr1 | 192,904,125 | 192,905,241 | 192,905,319 | 192,906,059 |