nsv6216550
- Organism: Homo sapiens
- Study:nstd214 (Naslavsky et al. 2022)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Naslavsky 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: 133 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 137 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6216550 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 165,708,162 | 165,708,162 | ||
| nsv6216550 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 165,677,399 | 165,677,399 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17867429 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17867429 | Submitted genomic | NC_000001.11:g.165 708162_165708163in sTCTCTCTCTCTGCCTCT CTCCCCGTCTCTCTCTCT CTGCCTCTCTCCCCG | GRCh38 (hg38) | NC_000001.11 | Chr1 | 165,708,162 | 165,708,162 | ||
| nssv17867429 | Remapped | Perfect | NC_000001.10:g.165 677399_165677400in sTCTCTCTCTCTGCCTCT CTCCCCGTCTCTCTCTCT CTGCCTCTCTCCCCG | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 165,677,399 | 165,677,399 |
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) |
|---|---|---|---|
| nssv17867429 | <0.001 | 1 | 1236 |