nsv5920105
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:75
- 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: 326 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 326 SVs from 28 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5920105 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 132,637,331 | 132,637,405 | ||
nsv5920105 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 134,450,835 | 134,450,909 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17354108 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17354108 | Submitted genomic | NC_000010.11:g.132 637331_132637405de l | GRCh38 (hg38) | NC_000010.11 | Chr10 | 132,637,331 | 132,637,405 | ||
nssv17354108 | Remapped | Perfect | NC_000010.10:g.134 450835_134450909de l | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 134,450,835 | 134,450,909 |