nsv5386490
- Organism: Homo sapiens
- Study:nstd186 (NCBI Curated Common Structural Variants)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:322
- Description:nsv4817779 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: 135 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 135 SVs from 38 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5386490 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 158,571,260 | 158,571,581 |
| nsv5386490 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 158,992,292 | 158,992,613 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16877970 | deletion | Curated | Curated |
| nssv16880828 | deletion | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16877970 | Remapped | Perfect | NC_000006.12:g.158 571260_158571581de l | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 158,571,260 | 158,571,581 |
| nssv16880828 | Remapped | Perfect | NC_000006.12:g.158 571260_158571581de l | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 158,571,260 | 158,571,581 |
| nssv16877970 | Submitted genomic | NC_000006.11:g.158 992292_158992613de l | GRCh37 (hg19) | NC_000006.11 | Chr6 | 158,992,292 | 158,992,613 | ||
| nssv16880828 | Submitted genomic | NC_000006.11:g.158 992292_158992613de l | GRCh37 (hg19) | NC_000006.11 | Chr6 | 158,992,292 | 158,992,613 |
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) |
|---|---|---|---|
| nssv16877970 | 0.101 | 1695 | 16834 |
| nssv16880828 | 0.098 | 156 | 1592 |