nsv6971301
- 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:34,541
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: 327 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 327 SVs from 59 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6971301 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 3,639,521 | 3,674,061 | ||
nsv6971301 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 3,689,522 | 3,724,062 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18401931 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18401931 | Submitted genomic | NC_000016.10:g.363 9521_3674061del | GRCh38 (hg38) | NC_000016.10 | Chr16 | 3,639,521 | 3,674,061 | ||
nssv18401931 | Remapped | Perfect | NC_000016.9:g.3689 522_3724062del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 3,689,522 | 3,724,062 |
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) |
---|---|---|---|
nssv18401931 | 1.8e-05 | 5 | 275998 |