nsv3071749
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:mobile element insertion
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Data Source:DEBNICK
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: 141 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3071749 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 63,488,531 | 63,488,531 |
| nsv3071749 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 61,565,892 | 61,565,892 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14038828 | mobile element insertion | PS206642_PA151796275_13813 | Curated | Curated |
| nssv14041281 | mobile element insertion | dcp1-ALU | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14038828 | Remapped | Perfect | NC_000017.11:g.634 88531_63488532ins2 88 | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 63,488,531 | 63,488,531 |
| nssv14041281 | Remapped | Perfect | NC_000017.11:g.634 88531_63488532ins? | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 63,488,531 | 63,488,531 |
| nssv14038828 | Submitted genomic | NC_000017.10:g.615 65892_61565893ins2 88 | GRCh37 (hg19) | NC_000017.10 | Chr17 | 61,565,892 | 61,565,892 | ||
| nssv14041281 | Submitted genomic | NC_000017.10:g.615 65892_61565893ins? | GRCh37 (hg19) | NC_000017.10 | Chr17 | 61,565,892 | 61,565,892 |