nsv3956075
- 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:18,166
- 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: 144 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 44 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3956075 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000012.12 | Chr12 | 110,701,211 | 110,719,376 | ||
| nsv3956075 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 111,139,016 | 111,157,181 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15216230 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv15216230 | Submitted genomic | NC_000012.12:g.(11 0701211_?)_(?_1107 19376)ins11348 | GRCh38 (hg38) | NC_000012.12 | Chr12 | 110,701,211 | 110,719,376 | ||
| nssv15216230 | Remapped | Perfect | NC_000012.11:g.(11 1139016_?)_(?_1111 57181)ins11348 | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 111,139,016 | 111,157,181 |