nsv4573318
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:2
- 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: 69 SVs from 4 studies. See in: genome view
Overlapping variant regions from other studies: 71 SVs from 4 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4573318 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 17,866,603 | 17,866,603 |
| nsv4573318 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000022.10 | Chr22 | 18,349,369 | 18,349,369 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16034007 | insertion | Sequencing | Other |
| nssv16034008 | insertion | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16034007 | Remapped | Perfect | NC_000022.11:g.178 66603_17866604ins5 1 | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 17,866,603 | 17,866,603 |
| nssv16034008 | Remapped | Perfect | NC_000022.11:g.178 66603_17866604ins5 1 | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 17,866,603 | 17,866,603 |
| nssv16034007 | Submitted genomic | NC_000022.10:g.183 49369_18349370ins5 1 | GRCh37.p13 | NC_000022.10 | Chr22 | 18,349,369 | 18,349,369 | ||
| nssv16034008 | Submitted genomic | NC_000022.10:g.183 49369_18349370ins5 1 | GRCh37.p13 | NC_000022.10 | Chr22 | 18,349,369 | 18,349,369 |
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) |
|---|---|---|---|
| nssv16034007 | <0.001 | 11 | 21254 |
| nssv16034008 | 0.003 | 64 | 21546 |