nsv4169834
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:69
- Publication(s):gnomAD_Structural_Variants
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: 39 SVs from 6 studies. See in: genome view
Overlapping variant regions from other studies: 39 SVs from 6 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4169834 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 66,921,205 | 66,921,273 |
nsv4169834 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000008.10 | Chr8 | 67,833,440 | 67,833,508 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15926506 | deletion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15926506 | Remapped | Perfect | NC_000008.11:g.669 21205_66921273del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 66,921,205 | 66,921,273 |
nssv15926506 | Submitted genomic | NC_000008.10:g.678 33440_67833508del | GRCh37.p13 | NC_000008.10 | Chr8 | 67,833,440 | 67,833,508 |
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) |
---|---|---|---|
nssv15926506 | 4.6e-005 | 1 | 21694 |