nsv4535341
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type: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: 95 SVs from 6 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 6 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4535341 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 21,487,434 | 21,487,434 |
| nsv4535341 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000024.9 | ChrY | 23,649,320 | 23,649,320 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16091015 | insertion | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16091015 | Remapped | Perfect | NC_000024.10:g.214 87434_21487435ins5 3 | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 21,487,434 | 21,487,434 |
| nssv16091015 | Submitted genomic | NC_000024.9:g.2364 9320_23649321ins53 | GRCh37.p13 | NC_000024.9 | ChrY | 23,649,320 | 23,649,320 |
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) |
|---|---|---|---|
| nssv16091015 | <0.001 | 2 | 11056 |