nsv5477723
- 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:14,755
- 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: 139 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 139 SVs from 34 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5477723 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 97,429,271 (-285, +62) | 97,444,025 (-106, +253) | ||
| nsv5477723 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 99,189,028 (-285, +62) | 99,203,782 (-106, +253) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17037609 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17037609 | Submitted genomic | NC_000010.11:g.(97 428986_97429333)_( 97443919_97444278) dup | GRCh38 (hg38) | NC_000010.11 | Chr10 | 97,429,271 (-285, +62) | 97,444,025 (-106, +253) | ||
| nssv17037609 | Remapped | Perfect | NC_000010.10:g.(99 188743_99189090)_( 99203676_99204035) dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 99,189,028 (-285, +62) | 99,203,782 (-106, +253) |
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) |
|---|---|---|---|
| nssv17037609 | <0.001 | 2 | 6404 |