esv8515
- 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:30,898
- 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: 555 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 555 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 208 SVs from 17 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
esv8515 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 159,133,024 | 159,133,024 | 159,163,921 | 159,163,921 |
esv8515 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 158,925,715 | 158,925,950 | 158,956,463 | 158,956,612 |
esv8515 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 158,618,476 | 158,618,711 | 158,649,224 | 158,649,373 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
essv30956 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
essv30956 | Remapped | Perfect | NC_000007.14:g.(15 9133024_159133024) _(159163921_159163 921)inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 159,133,024 | 159,133,024 | 159,163,921 | 159,163,921 |
essv30956 | Remapped | Perfect | NC_000007.13:g.(15 8925715_158925950) _(158956463_158956 612)inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 158,925,715 | 158,925,950 | 158,956,463 | 158,956,612 |
essv30956 | Submitted genomic | NC_000007.12:g.(15 8618476_158618711) _(158649224_158649 373)inv | NCBI36 (hg18) | NC_000007.12 | Chr7 | 158,618,476 | 158,618,711 | 158,649,224 | 158,649,373 |