nsv5463778
- 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:438,270
- 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: 1173 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 1173 SVs from 74 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5463778 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 90,479,596 (-24, +20) | 90,917,865 (-20, +24) | ||
| nsv5463778 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 89,775,413 (-24, +20) | 90,213,682 (-20, +24) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16971335 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16971335 | Submitted genomic | NC_000005.10:g.(90 479572_90479616)_( 90917845_90917889) del | GRCh38 (hg38) | NC_000005.10 | Chr5 | 90,479,596 (-24, +20) | 90,917,865 (-20, +24) | ||
| nssv16971335 | Remapped | Perfect | NC_000005.9:g.(897 75389_89775433)_(9 0213662_90213706)d el | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 89,775,413 (-24, +20) | 90,213,682 (-20, +24) |
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) |
|---|---|---|---|
| nssv16971335 | <0.001 | 1 | 6404 |