nsv6571992
- 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:519,881
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: 1619 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 1619 SVs from 80 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6571992 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000004.12 | Chr4 | 178,513,526 | 179,033,406 | ||
nsv6571992 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 179,434,680 | 179,954,560 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18264553 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18264553 | Submitted genomic | NC_000004.12:g.178 513526_179033406in v | GRCh38 (hg38) | NC_000004.12 | Chr4 | 178,513,526 | 179,033,406 | ||
nssv18264553 | Remapped | Perfect | NC_000004.11:g.179 434680_179954560in v | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 179,434,680 | 179,954,560 |
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) |
---|---|---|---|
nssv18264553 | <0.001 | 1 | 39304 |