nsv4440183
- Organism: Homo sapiens
- Study:nstd175 (Genome in a Bottle)
- Variant Type:delins
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,105
- Description:SVTYPE=DEL;REPTYPE=SUBSDEL
- Publication(s):Genome in a Bottle
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: 373 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 373 SVs from 61 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4440183 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 74,450,637 | 74,454,741 |
| nsv4440183 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 75,362,872 | 75,366,976 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15763161 | delins | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15763161 | Remapped | Perfect | NC_000008.11:g.744 50637_74454741deli nsCTACAATGTAATAACA TTGCCAAATAATT | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 74,450,637 | 74,454,741 |
| nssv15763161 | Submitted genomic | NC_000008.10:g.753 62872_75366976deli nsCTACAATGTAATAACA TTGCCAAATAATT | GRCh37 (hg19) | NC_000008.10 | Chr8 | 75,362,872 | 75,366,976 |