nsv4872414
- Organism: Homo sapiens
- Study:nstd200 (Abel et al. 2020)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:5,229,721
- Publication(s):Abel et al. 2020
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: 13357 SVs from 115 studies. See in: genome view
Overlapping variant regions from other studies: 13355 SVs from 115 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4872414 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 35,178,276 (+1) | 40,407,996 |
| nsv4872414 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 35,146,053 (+1) | 40,375,735 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16412137 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16412137 | Remapped | Good | NC_000006.12:g.(?_ 35178277)_40407996 inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 35,178,276 (+1) | 40,407,996 |
| nssv16412137 | Submitted genomic | NC_000006.11:g.(?_ 35146054)_40375735 inv | GRCh37 (hg19) | NC_000006.11 | Chr6 | 35,146,053 (+1) | 40,375,735 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16412137 | <0.001 | 1 | 16834 |