esv2421280
- Organism: Homo sapiens
- Study:estd194 (Bentley et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Bentley 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: 542 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 543 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 203 SVs from 8 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv2421280 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 31,589,099 | 31,589,099 |
esv2421280 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 31,607,216 | 31,607,216 |
esv2421280 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 31,517,137 | 31,517,137 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv4939084 | Remapped | Perfect | NC_000023.11:g.315 89099_31589100insA | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 31,589,099 | 31,589,099 |
essv4939084 | Remapped | Perfect | NC_000023.10:g.316 07216_31607217insA | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 31,607,216 | 31,607,216 |
essv4939084 | Submitted genomic | NC_000023.9:g.3151 7137_31517138insA | NCBI36 (hg18) | NC_000023.9 | ChrX | 31,517,137 | 31,517,137 |