nsv5655664
- 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: 299 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 302 SVs from 33 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5655664 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000013.11 | Chr13 | 113,728,306 | 113,728,306 | ||
| nsv5655664 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 114,431,279 | 114,431,279 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17097287 | insertion | SAMN00007824 | Sequencing | Sequence alignment | 1,699 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17097287 | Submitted genomic | NC_000013.11:g.113 728306_113728307in s144 | GRCh38 (hg38) | NC_000013.11 | Chr13 | 113,728,306 | 113,728,306 | ||
| nssv17097287 | Remapped | Perfect | NC_000013.10:g.114 431279_114431280in s144 | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 114,431,279 | 114,431,279 |