nsv5309676
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,100
- Publication(s):Chen et al. 2021
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: 236 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 56 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5309676 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000004.12 | Chr4 | 155,673,052 (-6, +5) | 155,677,151 (-5, +2) | ||
| nsv5309676 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 156,594,204 (-6, +5) | 156,598,303 (-5, +2) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16769692 | deletion | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16769692 | Submitted genomic | NC_000004.12:g.(15 5673046_155673057) _(155677146_155677 153)del | GRCh38.p13 | NC_000004.12 | Chr4 | 155,673,052 (-6, +5) | 155,677,151 (-5, +2) | ||
| nssv16769692 | Remapped | Perfect | NC_000004.11:g.(15 6594198_156594209) _(156598298_156598 305)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 156,594,204 (-6, +5) | 156,598,303 (-5, +2) |
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) |
|---|---|
| nssv16769692 | <0.001 |