nsv3964351
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:insertion
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:37,124
- Publication(s):Levy-Sakin et al. 2019
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: 239 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 239 SVs from 42 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3964351 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 134,411,366 | 134,448,489 | ||
| nsv3964351 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 133,747,057 | 133,784,180 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15214629 | insertion | Optical mapping | Optical mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15214629 | Submitted genomic | NC_000005.10:g.(13 4411366_?)_(?_1344 48489)ins2059 | GRCh38 (hg38) | NC_000005.10 | Chr5 | 134,411,366 | 134,448,489 | ||
| nssv15214629 | Remapped | Perfect | NC_000005.9:g.(133 747057_?)_(?_13378 4180)ins2059 | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 133,747,057 | 133,784,180 |