nsv6523675
- 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:794
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: 189 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 189 SVs from 27 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6523675 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000018.10 | Chr18 | 31,097,147 | 31,097,940 | ||
nsv6523675 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 28,677,110 | 28,677,903 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18039890 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18039890 | Submitted genomic | NC_000018.10:g.310 97147_31097940del | GRCh38 (hg38) | NC_000018.10 | Chr18 | 31,097,147 | 31,097,940 | ||
nssv18039890 | Remapped | Perfect | NC_000018.9:g.2867 7110_28677903del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 28,677,110 | 28,677,903 |
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) |
---|---|---|---|
nssv18039890 | 0.008 | 307 | 36368 |