nsv4755997
- 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:716,281
- 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: 2890 SVs from 98 studies. See in: genome view
Overlapping variant regions from other studies: 2890 SVs from 98 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4755997 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 26,600,555 | 27,316,835 |
| nsv4755997 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 26,889,484 | 27,605,764 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16287044 | inversion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16287044 | Remapped | Perfect | NC_000010.11:g.266 00555_27316835inv | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 26,600,555 | 27,316,835 |
| nssv16287044 | Submitted genomic | NC_000010.10:g.268 89484_27605764inv | GRCh37 (hg19) | NC_000010.10 | Chr10 | 26,889,484 | 27,605,764 |