nsv1588174
- 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:13
- Description:MOTIF=[T],NS=[301],REF=[13.0],RL=[13],RPA=[12.
0],RU=[T],QUAL=[126086] - 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: 62 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 62 SVs from 18 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1588174 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 61,791,260 | 61,791,272 |
| nsv1588174 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 61,558,732 | 61,558,744 |
Variant Call Information
| Variant Call ID | Type | Repeat Motif | Method | Analysis |
|---|---|---|---|---|
| nssv9348617 | short tandem repeat | (T) 12 | Sequencing | Genotyping |
| nssv9348618 | short tandem repeat | (T) 13 (ref) | Sequencing | Genotyping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv9348617 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 61,791,260 | 61,791,272 |
| nssv9348618 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 61,791,260 | 61,791,272 |
| nssv9348617 | Submitted genomic | GRCh37 (hg19) | NC_000011.9 | Chr11 | 61,558,732 | 61,558,744 | ||
| nssv9348618 | Submitted genomic | GRCh37 (hg19) | NC_000011.9 | Chr11 | 61,558,732 | 61,558,744 |