nsv4768211
- 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:28,797,588
- 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: 73592 SVs from 140 studies. See in: genome view
Overlapping variant regions from other studies: 73526 SVs from 140 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4768211 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 23,616,951 | 52,414,538 |
| nsv4768211 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 23,474,464 | 53,327,098 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16268730 | inversion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16268730 | Remapped | Good | NC_000008.11:g.236 16951_52414538inv | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 23,616,951 | 52,414,538 |
| nssv16268730 | Submitted genomic | NC_000008.10:g.234 74464_53327098inv | GRCh37 (hg19) | NC_000008.10 | Chr8 | 23,474,464 | 53,327,098 |