esv3808509
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:Chr13:g.42647252_47092439ins
- Publication(s):Forbes et al. 2008, Forbes et al. 2008
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: 148 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 25 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3808509 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 42,073,116 | 42,073,116 |
| esv3808509 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 46,518,304 | 46,518,304 |
| esv3808509 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 42,647,252 | 42,647,252 | ||
| esv3808509 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 47,092,439 | 47,092,439 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16637574 | insertion | 2197580 | Curated | Curated | 16 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16637574 | Remapped | Perfect | NC_000013.11:g.420 73116_42073117ins? NC_000013.11:g.465 18304_46518305ins? | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 42,073,116 | 42,073,116 |
| essv16637574 | Remapped | Perfect | NC_000013.11:g.420 73116_42073117ins? NC_000013.11:g.465 18304_46518305ins? | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 46,518,304 | 46,518,304 |
| essv16637574 | Submitted genomic | NC_000013.10:g.426 47252_42647253ins? NC_000013.10:g.470 92439_47092440ins? | GRCh37 (hg19) | NC_000013.10 | Chr13 | 42,647,252 | 42,647,252 | ||
| essv16637574 | Submitted genomic | NC_000013.10:g.426 47252_42647253ins? NC_000013.10:g.470 92439_47092440ins? | GRCh37 (hg19) | NC_000013.10 | Chr13 | 47,092,439 | 47,092,439 |