nsv6373585
- 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:443
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: 73 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 73 SVs from 15 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6373585 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 44,425,793 | 44,426,235 | ||
nsv6373585 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 44,467,285 | 44,467,727 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18209265 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18209265 | Submitted genomic | NC_000003.12:g.444 25793_44426235dup | GRCh38 (hg38) | NC_000003.12 | Chr3 | 44,425,793 | 44,426,235 | ||
nssv18209265 | Remapped | Perfect | NC_000003.11:g.444 67285_44467727dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 44,467,285 | 44,467,727 |
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) |
---|---|---|---|
nssv18209265 | <0.001 | 1 | 38136 |