nsv5979445
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,709
- Description:DESC=[BREAKPOINT2]
- Publication(s):Almarri et al. 2020
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: 1013 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 1014 SVs from 39 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5979445 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 1,288,436 | 1,292,144 | ||
nsv5979445 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 1,407,329 | 1,411,037 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17433808 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17433808 | Submitted genomic | NC_000023.11:g.128 8436_1292144inv | GRCh38 (hg38) | NC_000023.11 | ChrX | 1,288,436 | 1,292,144 | ||
nssv17433808 | Remapped | Perfect | NC_000023.10:g.140 7329_1411037inv | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 1,407,329 | 1,411,037 |