nsv426338
- Organism: Homo sapiens
- Study:nstd6 (Mills et al. 2006)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Mills et al. 2006
- TRACE: TRACE_NAME='G248P802295RA10.T0'
- TRACE: TRACE_NAME='S144P6426592FB12.T0.scf'
- TRACE: TRACE_NAME='S213P6240FE3.T0'
- TRACE: TRACE_NAME='S226P7175FC10.T0'
- TRACE: TRACE_NAME='S226P7579RE3.T0'
- TRACE: TRACE_NAME='S226P7933RE12.T0'
- TRACE: TRACE_NAME='S226P796RA4.T0'
- TRACE: TRACE_NAME='S249P7205FA3.T0'
- TRACE: TRACE_NAME='S249P7229FH7.T0'
- dbSNP: ss49906112
- Overlapping Genes
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: 349 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 359 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 1 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv426338 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 10,200,269 | 10,200,269 |
| nsv426338 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 10,037,878 | 10,037,878 |
| nsv426338 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000024.7 | ChrY | 10,631,239 | 10,631,239 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv444916 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv444916 | Remapped | Perfect | NC_000024.10:g.102 00269_10200270insC | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 10,200,269 | 10,200,269 |
| nssv444916 | Remapped | Perfect | NC_000024.9:g.1003 7878_10037879insC | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 10,037,878 | 10,037,878 |
| nssv444916 | Submitted genomic | NC_000024.7:g.1063 1239_10631240insC | NCBI35 (hg17) | NC_000024.7 | ChrY | 10,631,239 | 10,631,239 |