nsv3970418
- 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:167,889
- 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: 1015 SVs from 82 studies. See in: genome view
Overlapping variant regions from other studies: 1014 SVs from 82 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3970418 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 141,721,722 | 141,889,610 | ||
| nsv3970418 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 142,731,899 | 142,970,971 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15209693 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv15209693 | Submitted genomic | NC_000008.11:g.(14 1721722_?)_(?_1418 89610)ins3299 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 141,721,722 | 141,889,610 | ||
| nssv15209693 | Remapped | Pass | NC_000008.10:g.(14 2731899_?)_(?_1429 70971)ins3299 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 142,731,899 | 142,970,971 |