nsv6569908
- Organism: Homo sapiens
- Study:nstd223 (Sedlazeck et al. 2020)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,522
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: 89 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6569908 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 122,659,568 | 122,661,089 | ||
nsv6569908 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 125,421,847 | 125,423,368 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18279784 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18279784 | Submitted genomic | NC_000009.12:g.122 659568_122661089in v | GRCh38 (hg38) | NC_000009.12 | Chr9 | 122,659,568 | 122,661,089 | ||
nssv18279784 | Remapped | Perfect | NC_000009.11:g.125 421847_125423368in v | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 125,421,847 | 125,423,368 |
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) |
---|---|---|---|
nssv18279784 | <0.001 | 1 | 35918 |