nsv2070309
- Organism: Homo sapiens
- Study:nstd128 (Mallick et al. 2016)
- Variant Type:short tandem repeat
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21
- Description:MOTIF=[TAAA],NS=[301],REF=[5.25],RL=[21],RPA=[
6.25],RU=[TAAA],QUAL=[255778] - Publication(s):Mallick et al. 2016
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: 77 SVs from 11 studies. See in: genome view
Overlapping variant regions from other studies: 77 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv2070309 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 9,466,596 | 9,466,616 |
| nsv2070309 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 9,606,725 | 9,606,745 |
Variant Call Information
| Variant Call ID | Type | Repeat Motif | Method | Analysis |
|---|---|---|---|---|
| nssv10746777 | short tandem repeat | (TAAA) 6.25 | Sequencing | Genotyping |
| nssv10746778 | short tandem repeat | (TAAA) 5.25 (ref) | Sequencing | Genotyping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv10746777 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 9,466,596 | 9,466,616 |
| nssv10746778 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 9,466,596 | 9,466,616 |
| nssv10746777 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 9,606,725 | 9,606,745 | ||
| nssv10746778 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 9,606,725 | 9,606,745 |