nsv5976228
- 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:161,513
- Description:DESC=[BREAKPOINT1]
- 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: 718 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 729 SVs from 79 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5976228 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 57,665,629 | 57,827,141 | ||
nsv5976228 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 57,725,335 | 57,886,847 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17447398 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17447398 | Submitted genomic | NC_000007.14:g.576 65629_57827141inv | GRCh38 (hg38) | NC_000007.14 | Chr7 | 57,665,629 | 57,827,141 | ||
nssv17447398 | Remapped | Perfect | NC_000007.13:g.577 25335_57886847inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 57,725,335 | 57,886,847 |