nsv6403869
- 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:495,000
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: 1501 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 944 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 475 SVs from 40 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6403869 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 141,059,401 | 141,554,400 | ||
| nsv6403869 | Remapped | Pass | GRCh37.p13 | Primary Assembly | Second Pass | NC_000005.9 | Chr5 | 140,438,986 | 140,687,716 |
| nsv6403869 | Remapped | Pass | GRCh37.p13 | PATCHES | First Pass | NW_004775428.1 | Chr5|NW_00 4775428.1 | 294,577 | 543,325 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18213359 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18213359 | Submitted genomic | NC_000005.10:g.141 059401_141554400du p | GRCh38 (hg38) | NC_000005.10 | Chr5 | 141,059,401 | 141,554,400 | ||
| nssv18213359 | Remapped | Pass | NW_004775428.1:g.2 94577_543325dup | GRCh37.p13 | First Pass | NW_004775428.1 | Chr5|NW_00 4775428.1 | 294,577 | 543,325 |
| nssv18213359 | Remapped | Pass | NC_000005.9:g.1404 38986_140687716dup | GRCh37.p13 | Second Pass | NC_000005.9 | Chr5 | 140,438,986 | 140,687,716 |
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) |
|---|---|---|---|
| nssv18213359 | <0.001 | 34 | 39246 |