nsv3109632
- Organism: Homo sapiens
- Study:nstd144 (Gardner et al. 2017)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:TSD=AAGAAACGTTGC;INTERNAL=NM_004466,INTRONIC;M
EINFO=AluYa5,0,281,+ - Publication(s):Gardner et al. 2017
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: 258 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 258 SVs from 34 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3109632 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 92,172,985 | 92,172,985 |
| nsv3109632 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 92,825,238 | 92,825,238 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv14060382 | alu insertion | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14060382 | Remapped | Perfect | NC_000013.11:g.921 72985_92172986ins2 81 | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 92,172,985 | 92,172,985 |
| nssv14060382 | Submitted genomic | NC_000013.10:g.928 25238_92825239ins2 81 | GRCh37 (hg19) | NC_000013.10 | Chr13 | 92,825,238 | 92,825,238 |
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) |
|---|---|
| nssv14060382 | 0.294 |