nsv5615002
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Ebert et al. 2021
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: 453 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 449 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 40 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5615002 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 154,773,843 | 154,773,843 | ||
| nsv5615002 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000023.10 | ChrX | 154,002,118 | 154,002,118 |
| nsv5615002 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871103.3 | ChrX|NW_00 3871103.3 | 2,207,822 | 2,207,822 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17166298 | Submitted genomic | NC_000023.11:g.154 773843_154773844in s128 | GRCh38 (hg38) | NC_000023.11 | ChrX | 154,773,843 | 154,773,843 | ||
| nssv17166298 | Remapped | Perfect | NW_003871103.3:g.2 207822_2207823ins1 28 | GRCh37.p13 | First Pass | NW_003871103.3 | ChrX|NW_00 3871103.3 | 2,207,822 | 2,207,822 |
| nssv17166298 | Remapped | Perfect | NC_000023.10:g.154 002118_154002119in s128 | GRCh37.p13 | Second Pass | NC_000023.10 | ChrX | 154,002,118 | 154,002,118 |