nsv4751153
- Organism: Homo sapiens
- Study:nstd199 (Quan et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Quan 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: 128 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 37 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 39 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 41 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4751153 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 7,844,549 | 7,844,549 |
| nsv4751153 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187583.1 | Chr11|NT_1 87583.1 | 65,423 | 65,423 |
| nsv4751153 | Remapped | Perfect | GRCh38.p12 | PATCHES | Second Pass | NW_011332695.1 | Chr11|NW_0 11332695.1 | 75,543 | 75,543 |
| nsv4751153 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 7,866,096 | 7,866,096 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16280546 | insertion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16280546 | Remapped | Perfect | NT_187583.1:g.6542 3_65424ins10377 | GRCh38.p12 | Second Pass | NT_187583.1 | Chr11|NT_1 87583.1 | 65,423 | 65,423 |
| nssv16280546 | Remapped | Perfect | NW_011332695.1:g.7 5543_75544ins10377 | GRCh38.p12 | Second Pass | NW_011332695.1 | Chr11|NW_0 11332695.1 | 75,543 | 75,543 |
| nssv16280546 | Remapped | Perfect | NC_000011.10:g.784 4549_7844550ins103 77 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 7,844,549 | 7,844,549 |
| nssv16280546 | Submitted genomic | NC_000011.9:g.7866 096_7866097ins1037 7 | GRCh37 (hg19) | NC_000011.9 | Chr11 | 7,866,096 | 7,866,096 |