nsv4751400
- Organism: Homo sapiens
- Study:nstd199 (Quan et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:217,984,224
- 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: 495924 SVs from 163 studies. See in: genome view
Overlapping variant regions from other studies: 494402 SVs from 163 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4751400 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 16,799,162 | 234,783,385 |
| nsv4751400 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 17,125,657 | 234,919,132 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16295980 | inversion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16295980 | Remapped | Good | NC_000001.11:g.167 99162_234783385inv | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 16,799,162 | 234,783,385 |
| nssv16295980 | Submitted genomic | NC_000001.10:g.171 25657_234919132inv | GRCh37 (hg19) | NC_000001.10 | Chr1 | 17,125,657 | 234,919,132 |