nsv5627640
- 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: 189 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 197 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 39 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv5627640 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 50,066,625 | 50,066,625 | ||
| nsv5627640 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000010.10 | Chr10 | 51,826,385 | 51,826,385 |
| nsv5627640 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004504302.1 | Chr10|NW_0 04504302.1 | 245,800 | 245,800 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17070805 | insertion | SAMN00006579 | Sequencing | Sequence alignment | 23,265 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17070805 | Submitted genomic | NC_000010.11:g.500 66625_50066626ins9 43 | GRCh38 (hg38) | NC_000010.11 | Chr10 | 50,066,625 | 50,066,625 | ||
| nssv17070805 | Remapped | Perfect | NW_004504302.1:g.2 45800_245801ins943 | GRCh37.p13 | First Pass | NW_004504302.1 | Chr10|NW_0 04504302.1 | 245,800 | 245,800 |
| nssv17070805 | Remapped | Perfect | NC_000010.10:g.518 26385_51826386ins9 43 | GRCh37.p13 | Second Pass | NC_000010.10 | Chr10 | 51,826,385 | 51,826,385 |