nsv5499838
- 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:81,444
- 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: 358 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 358 SVs from 48 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5499838 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 103,167,084 (-20, +24) | 103,248,527 (-25, +20) | ||
| nsv5499838 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 104,926,841 (-20, +24) | 105,008,284 (-25, +20) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17039989 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17039989 | Submitted genomic | NC_000010.11:g.(10 3167064_103167108) _(103248502_103248 547)dup | GRCh38 (hg38) | NC_000010.11 | Chr10 | 103,167,084 (-20, +24) | 103,248,527 (-25, +20) | ||
| nssv17039989 | Remapped | Perfect | NC_000010.10:g.(10 4926821_104926865) _(105008259_105008 304)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 104,926,841 (-20, +24) | 105,008,284 (-25, +20) |
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) |
|---|---|---|---|
| nssv17039989 | <0.001 | 1 | 6404 |