nsv6985050
- Organism: Homo sapiens
- Study:nstd229 (Jun et al. 2023)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,625
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: 512 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 512 SVs from 47 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6985050 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 29,967,581 | 29,970,205 | ||
nsv6985050 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 29,978,902 | 29,981,526 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18398554 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18398554 | Submitted genomic | NC_000016.10:g.299 67581_29970205del | GRCh38 (hg38) | NC_000016.10 | Chr16 | 29,967,581 | 29,970,205 | ||
nssv18398554 | Remapped | Perfect | NC_000016.9:g.2997 8902_29981526del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 29,978,902 | 29,981,526 |
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) |
---|---|---|---|
nssv18398554 | 4.3e-05 | 12 | 275750 |