nsv3565656
- Organism: Homo sapiens
- Study:nstd152 (Chaisson et al. 2019)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:Insertion of a SVA mobile element relative to the reference
- Publication(s):Chaisson 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: 149 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 39 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3565656 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 109,650,355 (-15, +15) | 109,650,355 (-15, +15) | ||
nsv3565656 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 112,412,635 (-15, +15) | 112,412,635 (-15, +15) |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14348327 | Submitted genomic | NC_000009.12:g.(10 9650340_109650370) _(109650340_109650 370)ins508 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 109,650,355 (-15, +15) | 109,650,355 (-15, +15) | ||
nssv14348327 | Remapped | Perfect | NC_000009.11:g.(11 2412620_112412650) _(112412620_112412 650)ins508 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 112,412,635 (-15, +15) | 112,412,635 (-15, +15) |