nsv5447095
- Organism: Homo sapiens
- Study:nstd206 (Byrska-Bishop et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:552
- 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: 196 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 196 SVs from 27 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5447095 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000002.12 | Chr2 | 61,413,445 | 61,413,996 | ||
| nsv5447095 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 61,640,580 | 61,641,131 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16914900 | deletion | Sequencing | Sequence alignment |
| nssv16914901 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16914900 | Submitted genomic | NC_000002.12:g.614 13445_61413996del | GRCh38 (hg38) | NC_000002.12 | Chr2 | 61,413,445 | 61,413,996 | ||
| nssv16914901 | Submitted genomic | NC_000002.12:g.614 13445_61413996dup | GRCh38 (hg38) | NC_000002.12 | Chr2 | 61,413,445 | 61,413,996 | ||
| nssv16914900 | Remapped | Perfect | NC_000002.11:g.616 40580_61641131del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 61,640,580 | 61,641,131 |
| nssv16914901 | Remapped | Perfect | NC_000002.11:g.616 40580_61641131dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 61,640,580 | 61,641,131 |
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) |
|---|---|---|---|
| nssv16914900 | <0.001 | 6 | 6400 |
| nssv16914901 | <0.001 | 3 | 6404 |