nsv3964110
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:inversion
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:33,050
- 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: 349 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 349 SVs from 42 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3964110 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000013.11 | Chr13 | 79,842,095 | 79,875,144 | ||
| nsv3964110 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 80,416,230 | 80,449,279 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15206786 | inversion | Optical mapping | Optical mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15206786 | Submitted genomic | NC_000013.11:g.(79 842095_?)_(?_79875 144)inv | GRCh38 (hg38) | NC_000013.11 | Chr13 | 79,842,095 | 79,875,144 | ||
| nssv15206786 | Remapped | Perfect | NC_000013.10:g.(80 416230_?)_(?_80449 279)inv | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 80,416,230 | 80,449,279 |