nsv6789367
- 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:1,233,132
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: 2832 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 2818 SVs from 96 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6789367 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 48,645,525 | 49,878,656 | ||
nsv6789367 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 48,613,261 | 49,846,369 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18715831 | duplication | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18715831 | Submitted genomic | NC_000006.12:g.486 45525_49878656dup | GRCh38 (hg38) | NC_000006.12 | Chr6 | 48,645,525 | 49,878,656 | ||
nssv18715831 | Remapped | Good | NC_000006.11:g.486 13261_49846369dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 48,613,261 | 49,846,369 |
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) |
---|---|---|---|
nssv18715831 | 4e-06 | 1 | 270702 |