nsv1148
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:34,642
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 250 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 250 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 7 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1148 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 100,691,554 | 100,726,195 |
| nsv1148 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 101,343,808 | 101,378,449 |
| nsv1148 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000013.9 | Chr13 | 100,141,809 | 100,176,450 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1166 | Remapped | Perfect | NC_000013.11:g.(10 0691554_?)_(?_1007 26195)ins6356 | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 100,691,554 | 100,726,195 |
| nssv1166 | Remapped | Perfect | NC_000013.10:g.(10 1343808_?)_(?_1013 78449)ins6356 | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 101,343,808 | 101,378,449 |
| nssv1166 | Submitted genomic | NC_000013.9:g.(100 141809_?)_(?_10017 6450)ins6356 | NCBI35 (hg17) | NC_000013.9 | Chr13 | 100,141,809 | 100,176,450 |