nsv7141622
- Organism: Homo sapiens
- Study:nstd232 (Keane et al. 2023)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
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: 155 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 155 SVs from 52 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7141622 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 59,420,699 | 59,420,699 |
| nsv7141622 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000015.9 | Chr15 | 59,712,898 | 59,712,898 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18836844 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18836844 | Remapped | Perfect | NC_000015.10:g.594 20699_59420700insG AAGAACGTGCTCTACTGT GTTCTGGTGGGGTCACGT TCTCTAGGCCAG | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 59,420,699 | 59,420,699 |
| nssv18836844 | Submitted genomic | NC_000015.9:g.5971 2898_59712899insGA AGAACGTGCTCTACTGTG TTCTGGTGGGGTCACGTT CTCTAGGCCAG | GRCh37.p13 | NC_000015.9 | Chr15 | 59,712,898 | 59,712,898 |
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) |
|---|---|---|---|
| nssv18836844 | 1 | 2 | 2 |