nsv6793048
- Organism: Homo sapiens
- Study:nstd229 (Jun et al. 2023)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:35,689
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: 208 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 204 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 40 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6793048 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 140,874,905 | 140,910,593 | ||
| nsv6793048 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000005.9 | Chr5 | 140,254,490 | 140,290,178 |
| nsv6793048 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004775428.1 | Chr5|NW_00 4775428.1 | 110,081 | 145,769 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18695583 | duplication | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18695583 | Submitted genomic | NC_000005.10:g.140 874905_140910593du p | GRCh38 (hg38) | NC_000005.10 | Chr5 | 140,874,905 | 140,910,593 | ||
| nssv18695583 | Remapped | Perfect | NW_004775428.1:g.1 10081_145769dup | GRCh37.p13 | First Pass | NW_004775428.1 | Chr5|NW_00 4775428.1 | 110,081 | 145,769 |
| nssv18695583 | Remapped | Perfect | NC_000005.9:g.1402 54490_140290178dup | GRCh37.p13 | Second Pass | NC_000005.9 | Chr5 | 140,254,490 | 140,290,178 |
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) |
|---|---|---|---|
| nssv18695583 | 4e-06 | 1 | 275094 |