nsv6138597
- Organism: Homo sapiens
- Study:nstd206 (Byrska-Bishop et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,278
- Publication(s):Byrska-Bishop et al. 2022
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: 112 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 112 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6138597 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 92,230,807 (-10, +9) | 92,232,084 (-10, +9) | ||
| nsv6138597 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 92,696,364 (-10, +9) | 92,697,641 (-10, +9) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16906464 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16906464 | Submitted genomic | NC_000001.11:g.(92 230797_92230816)_( 92232074_92232093) dup | GRCh38 (hg38) | NC_000001.11 | Chr1 | 92,230,807 (-10, +9) | 92,232,084 (-10, +9) | ||
| nssv16906464 | Remapped | Perfect | NC_000001.10:g.(92 696354_92696373)_( 92697631_92697650) dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 92,696,364 (-10, +9) | 92,697,641 (-10, +9) |
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) |
|---|---|---|---|
| nssv16906464 | <0.001 | 1 | 6404 |