nsv3176563
- Organism: Homo sapiens
- Study:nstd152 (Chaisson et al. 2019)
- Variant Type:mobile element deletion
- Method Type:Optical mapping, Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:11,365
- Description:Absence of a AluY mobile element insertion that is present in the reference
- Publication(s):Chaisson et al. 2019
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: 306 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 386 SVs from 58 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3176563 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 38,863,133 | 38,874,497 | ||
| nsv3176563 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 38,863,130 | 38,874,494 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14438592 | alu deletion | HG00514 | Optical mapping, Sequencing | Optical mapping, Sequence alignment, de novo and local sequence assembly | 39,861 |
| nssv14439174 | alu deletion | SAMN00006581 | Optical mapping, Sequencing | Optical mapping, Sequence alignment, de novo and local sequence assembly | 41,185 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14438592 | Submitted genomic | NC_000009.12:g.388 63133_38874497del1 1364 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 38,863,133 | 38,874,497 | ||
| nssv14439174 | Submitted genomic | NC_000009.12:g.388 63133_38874497del1 1364 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 38,863,133 | 38,874,497 | ||
| nssv14438592 | Remapped | Perfect | NC_000009.11:g.388 63130_38874494del1 1364 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 38,863,130 | 38,874,494 |
| nssv14439174 | Remapped | Perfect | NC_000009.11:g.388 63130_38874494del1 1364 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 38,863,130 | 38,874,494 |