esv1679496
- 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:13,200
- 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: 573 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 315 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 571 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 26 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv1679496 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 49,715,000 | 49,728,196 |
esv1679496 | Remapped | Good | GRCh38.p12 | PATCHES | Second Pass | NW_019805495.1 | Chr11|NW_0 19805495.1 | 179,146 | 192,345 |
esv1679496 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 49,736,552 | 49,749,748 |
esv1679496 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 49,693,128 | 49,706,324 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv4272661 | Remapped | Good | NW_019805495.1:g.1 79146_192345inv | GRCh38.p12 | Second Pass | NW_019805495.1 | Chr11|NW_0 19805495.1 | 179,146 | 192,345 |
essv4272661 | Remapped | Perfect | NC_000011.10:g.497 15000_49728196inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 49,715,000 | 49,728,196 |
essv4272661 | Remapped | Perfect | NC_000011.9:g.4973 6552_49749748inv | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 49,736,552 | 49,749,748 |
essv4272661 | Submitted genomic | NC_000011.8:g.4969 3128_49706324inv | NCBI36 (hg18) | NC_000011.8 | Chr11 | 49,693,128 | 49,706,324 |