nsv4533989
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):gnomAD_Structural_Variants
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: 153 SVs from 10 studies. See in: genome view
Overlapping variant regions from other studies: 3 SVs from 2 studies. See in: genome view
Overlapping variant regions from other studies: 151 SVs from 10 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4533989 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 80,012,124 | 80,012,124 |
| nsv4533989 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187635.1 | ChrX|NT_18 7635.1 | 84,959 | 84,959 |
| nsv4533989 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000023.10 | ChrX | 79,267,623 | 79,267,623 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16088226 | insertion | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16088226 | Remapped | Perfect | NT_187635.1:g.8495 9_84960ins77 | GRCh38.p12 | Second Pass | NT_187635.1 | ChrX|NT_18 7635.1 | 84,959 | 84,959 |
| nssv16088226 | Remapped | Perfect | NC_000023.11:g.800 12124_80012125ins7 7 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 80,012,124 | 80,012,124 |
| nssv16088226 | Submitted genomic | NC_000023.10:g.792 67623_79267624ins7 7 | GRCh37.p13 | NC_000023.10 | ChrX | 79,267,623 | 79,267,623 |
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) |
|---|---|---|---|
| nssv16088226 | 4.7e-005 | 1 | 21432 |