esv2594391
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,185
- Description:originalFile=Yoruban_large_indels_8.4x.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: 487 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 489 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 279 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 | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2594391 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 2,813,485 | 2,814,669 |
| esv2594391 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 2,813,485 | 2,814,669 |
| esv2594391 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 2,803,485 | 2,804,669 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5298363 | Remapped | Perfect | NC_000009.12:g.(28 13485_?)_(?_281466 9)ins? | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 2,813,485 | 2,814,669 |
| essv5298363 | Remapped | Perfect | NC_000009.11:g.(28 13485_?)_(?_281466 9)ins? | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 2,813,485 | 2,814,669 |
| essv5298363 | Submitted genomic | NC_000009.10:g.(28 03485_?)_(?_280466 9)ins? | NCBI36 (hg18) | NC_000009.10 | Chr9 | 2,803,485 | 2,804,669 |