nsv5383380
- Organism: Homo sapiens
- Study:nstd186 (NCBI Curated Common Structural Variants)
- Variant Type:mobile element deletion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:312
- Description:nsv4879641 from Abel et. al 2020. For a full list of variants now included in nstd186, refer to the mapping file provided here.
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: 160 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 160 SVs from 57 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5383380 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 126,640,095 | 126,640,406 |
| nsv5383380 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 126,358,938 | 126,359,249 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16875838 | alu deletion | Curated | Curated |
| nssv16885272 | alu deletion | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16875838 | Remapped | Perfect | NC_000003.12:g.126 640095_126640406de l | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 126,640,095 | 126,640,406 |
| nssv16885272 | Remapped | Perfect | NC_000003.12:g.126 640095_126640406de l | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 126,640,095 | 126,640,406 |
| nssv16875838 | Submitted genomic | NC_000003.11:g.126 358938_126359249de l | GRCh37 (hg19) | NC_000003.11 | Chr3 | 126,358,938 | 126,359,249 | ||
| nssv16885272 | Submitted genomic | NC_000003.11:g.126 358938_126359249de l | GRCh37 (hg19) | NC_000003.11 | Chr3 | 126,358,938 | 126,359,249 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16875838 | 0.748 | 21882 | 29246 |
| nssv16885272 | 0.746 | 12552 | 16834 |