nsv3967881
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:insertion
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:28,574
- Publication(s):Levy-Sakin et al. 2019
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: 225 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 225 SVs from 46 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3967881 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 119,522,699 | 119,551,272 | ||
| nsv3967881 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 121,282,211 | 121,310,784 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15222201 | insertion | Optical mapping | Optical mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15222201 | Submitted genomic | NC_000010.11:g.(11 9522699_?)_(?_1195 51272)ins2076 | GRCh38 (hg38) | NC_000010.11 | Chr10 | 119,522,699 | 119,551,272 | ||
| nssv15222201 | Remapped | Perfect | NC_000010.10:g.(12 1282211_?)_(?_1213 10784)ins2076 | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 121,282,211 | 121,310,784 |