esv1505928
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:10,056
- Publication(s):Levy et al. 2007
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: 195 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 206 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 31 SVs from 14 studies. See in: genome view
Overlapping variant regions from other studies: 83 SVs from 14 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv1505928 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 47,306,914 | 47,316,969 |
esv1505928 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 48,214,931 | 48,226,228 |
esv1505928 | Remapped | Pass | GRCh37.p13 | PATCHES | Second Pass | NW_004775431.1 | Chr8|NW_00 4775431.1 | 43,072 | 53,127 |
esv1505928 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 48,377,484 | 48,388,781 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv3641514 | Remapped | Pass | NC_000008.11:g.473 06914_47316969inv | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 47,306,914 | 47,316,969 |
essv3641514 | Remapped | Pass | NW_004775431.1:g.4 3072_53127inv | GRCh37.p13 | Second Pass | NW_004775431.1 | Chr8|NW_00 4775431.1 | 43,072 | 53,127 |
essv3641514 | Remapped | Perfect | NC_000008.10:g.482 14931_48226228inv | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 48,214,931 | 48,226,228 |
essv3641514 | Submitted genomic | NC_000008.9:g.4837 7484_48388781inv | NCBI36 (hg18) | NC_000008.9 | Chr8 | 48,377,484 | 48,388,781 |