esv6524
- Organism: Homo sapiens
- Study:estd19 (Ahn et al. 2009)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,464
- Publication(s):Ahn 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: 443 SVs from 66 studies. See in: genome view
Overlapping variant regions from other studies: 443 SVs from 66 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv6524 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 156,594,388 | 156,594,516 | 156,601,629 | 156,601,851 |
| esv6524 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 156,387,082 | 156,387,210 | 156,394,323 | 156,394,545 |
| esv6524 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 156,079,843 | 156,079,971 | 156,087,084 | 156,087,306 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv28965 | inversion | Sequencing | Read depth and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv28965 | Remapped | Perfect | NC_000007.14:g.(15 6594388_156594516) _(156601629_156601 851)inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 156,594,388 | 156,594,516 | 156,601,629 | 156,601,851 |
| essv28965 | Remapped | Perfect | NC_000007.13:g.(15 6387082_156387210) _(156394323_156394 545)inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 156,387,082 | 156,387,210 | 156,394,323 | 156,394,545 |
| essv28965 | Submitted genomic | NC_000007.12:g.(15 6079843_156079971) _(156087084_156087 306)inv | NCBI36 (hg18) | NC_000007.12 | Chr7 | 156,079,843 | 156,079,971 | 156,087,084 | 156,087,306 |