nsv6650228
- 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:109,839
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: 418 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 418 SVs from 46 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6650228 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 43,699,713 | 43,809,551 | ||
nsv6650228 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 44,165,384 | 44,275,222 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18629181 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18629181 | Submitted genomic | NC_000001.11:g.436 99713_43809551dup | GRCh38 (hg38) | NC_000001.11 | Chr1 | 43,699,713 | 43,809,551 | ||
nssv18629181 | Remapped | Perfect | NC_000001.10:g.441 65384_44275222dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 44,165,384 | 44,275,222 |
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) |
---|---|---|---|
nssv18629181 | 4e-06 | 1 | 275390 |