nsv3071846
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Data Source:HUMANGENOME_JCVI
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: 235 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 235 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3071846 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 127,850,004 | 127,850,004 |
| nsv3071846 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 128,862,250 | 128,862,250 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14042353 | insertion | 1104685372005 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14042353 | Remapped | Perfect | NC_000008.11:g.127 850004_127850005in s255 | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 127,850,004 | 127,850,004 |
| nssv14042353 | Submitted genomic | NC_000008.10:g.128 862250_128862251in s255 | GRCh37 (hg19) | NC_000008.10 | Chr8 | 128,862,250 | 128,862,250 |