nsv286
- Organism: Homo sapiens
- Study:nstd1 (Tuzun et al. 2005)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,128
- Publication(s):Tuzun et al. 2005
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 157 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 157 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 3 SVs from 3 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv286 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 72,087,810 | 72,106,937 |
nsv286 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 72,797,513 | 72,816,640 |
nsv286 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000006.9 | Chr6 | 72,854,234 | 72,873,361 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv286 | insertion | SAMN00000376 | Sequencing | Paired-end mapping | 297 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv286 | Remapped | Perfect | NC_000006.12:g.(72 087810_?)_(?_72106 937)ins9070 | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 72,087,810 | 72,106,937 |
nssv286 | Remapped | Perfect | NC_000006.11:g.(72 797513_?)_(?_72816 640)ins9070 | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 72,797,513 | 72,816,640 |
nssv286 | Submitted genomic | NC_000006.9:g.(728 54234_?)_(?_728733 61)ins9070 | NCBI35 (hg17) | NC_000006.9 | Chr6 | 72,854,234 | 72,873,361 |