esv3666948
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:98
- Publication(s):Besenbacher et al. 2015
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: 360 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 360 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 |
---|---|---|---|---|---|---|---|---|---|
esv3666948 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 71,469,613 | 71,469,710 |
esv3666948 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 70,689,463 | 70,689,560 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
essv16489457 | inversion | Sequencing | de novo sequence assembly |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv16489457 | Remapped | Perfect | NC_000023.11:g.714 69613_71469710inv9 7 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 71,469,613 | 71,469,710 |
essv16489457 | Submitted genomic | NC_000023.10:g.706 89463_70689560inv9 7 | GRCh37 (hg19) | NC_000023.10 | ChrX | 70,689,463 | 70,689,560 |