nsv6451819
- Organism: Homo sapiens
- Study:nstd223 (Sedlazeck et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:151,200
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: 451 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 451 SVs from 61 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6451819 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 73,597,801 | 73,749,000 | ||
nsv6451819 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 75,357,559 | 75,508,758 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18186519 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18186519 | Submitted genomic | NC_000010.11:g.735 97801_73749000dup | GRCh38 (hg38) | NC_000010.11 | Chr10 | 73,597,801 | 73,749,000 | ||
nssv18186519 | Remapped | Perfect | NC_000010.10:g.753 57559_75508758dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 75,357,559 | 75,508,758 |
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) |
---|---|---|---|
nssv18186519 | <0.001 | 14 | 37212 |