nsv3067122
- Organism: Homo sapiens
- Study:nstd142 (Rahbari et al. 2017)
- Variant Type:sequence alteration
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,440
- Description:
NC_000001.9:g.159888397_159890836con159806551_159808988 - Publication(s):Rahbari 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: 421 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 425 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 202 SVs from 29 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3067122 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 161,651,983 | 161,654,422 |
| nsv3067122 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 161,621,773 | 161,624,212 |
| nsv3067122 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 159,888,397 | 159,890,836 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14038728 | sequence alteration | NA18956 | Sequencing | Sequence alignment | nssv14038725 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv14038728 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 161,651,983 | 161,654,422 |
| nssv14038728 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 161,621,773 | 161,624,212 |
| nssv14038728 | Submitted genomic | NCBI36 (hg18) | NC_000001.9 | Chr1 | 159,888,397 | 159,890,836 |