nsv5200270
- Organism: Homo sapiens
- Study:nstd205 (Kwong et al. 2021)
- Variant Type:delins
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,243
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: 123 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 29 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5200270 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 32,372,756 | 32,376,998 |
| nsv5200270 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000013.10 | Chr13 | 32,946,893 | 32,951,135 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv16736573 | delins | 13 | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16736573 | Remapped | Perfect | NC_000013.11:g.323 72756_32376998deli ns? | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 32,372,756 | 32,376,998 |
| nssv16736573 | Submitted genomic | NC_000013.10:g.329 46893_32951135deli ns? | GRCh37.p13 | NC_000013.10 | Chr13 | 32,946,893 | 32,951,135 |