nsv3067438
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:delins
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,850
- 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: 537 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 537 SVs from 48 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3067438 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 46,292,807 | 46,294,656 |
| nsv3067438 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000021.8 | Chr21 | 47,712,721 | 47,714,570 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14042639 | delins | 1104685167528 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14042639 | Remapped | Perfect | NC_000021.9:g.4629 2807_46294656delin s1184 | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 46,292,807 | 46,294,656 |
| nssv14042639 | Submitted genomic | NC_000021.8:g.4771 2721_47714570delin s1184 | GRCh37 (hg19) | NC_000021.8 | Chr21 | 47,712,721 | 47,714,570 |