nsv4492557
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):gnomAD_Structural_Variants
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: 178 SVs from 8 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 1 studies. See in: genome view
Overlapping variant regions from other studies: 178 SVs from 8 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4492557 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 7,496,565 | 7,496,565 |
| nsv4492557 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NW_003315928.1 | Chr9|NW_00 3315928.1 | 82,384 | 82,384 |
| nsv4492557 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000009.11 | Chr9 | 7,496,565 | 7,496,565 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16082457 | alu insertion | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16082457 | Remapped | Perfect | NW_003315928.1:g.8 2384_82385ins280 | GRCh38.p12 | Second Pass | NW_003315928.1 | Chr9|NW_00 3315928.1 | 82,384 | 82,384 |
| nssv16082457 | Remapped | Perfect | NC_000009.12:g.749 6565_7496566ins280 | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 7,496,565 | 7,496,565 |
| nssv16082457 | Submitted genomic | NC_000009.11:g.749 6565_7496566ins280 | GRCh37.p13 | NC_000009.11 | Chr9 | 7,496,565 | 7,496,565 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16082457 | 4.6e-005 | 1 | 21694 |