nsv4256093
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:474
- 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: 28 SVs from 12 studies. See in: genome view
Overlapping variant regions from other studies: 5 SVs from 4 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view
Overlapping variant regions from other studies: 26 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4256093 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 46,810,816 | 46,811,289 |
| nsv4256093 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_2 | Second Pass | NT_187663.1 | Chr17|NT_1 87663.1 | 1,330,234 | 1,330,707 |
| nsv4256093 | Remapped | Pass | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_167251.2 | Chr17|NT_1 67251.2 | 1,796,709 | 1,797,015 |
| nsv4256093 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000017.10 | Chr17 | 44,888,182 | 44,888,655 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15833869 | deletion | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15833869 | Remapped | Perfect | NT_187663.1:g.1330 234_1330707del | GRCh38.p12 | Second Pass | NT_187663.1 | Chr17|NT_1 87663.1 | 1,330,234 | 1,330,707 |
| nssv15833869 | Remapped | Pass | NT_167251.2:g.1796 709_1797015del | GRCh38.p12 | Second Pass | NT_167251.2 | Chr17|NT_1 67251.2 | 1,796,709 | 1,797,015 |
| nssv15833869 | Remapped | Perfect | NC_000017.11:g.468 10816_46811289del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 46,810,816 | 46,811,289 |
| nssv15833869 | Submitted genomic | NC_000017.10:g.448 88182_44888655del | GRCh37.p13 | NC_000017.10 | Chr17 | 44,888,182 | 44,888,655 |
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) |
|---|---|---|---|
| nssv15833869 | 0.137 | 2975 | 21690 |