nsv5953983
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Almarri et al. 2020
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: 124 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 124 SVs from 20 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5953983 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000002.12 | Chr2 | 223,789,812 | 223,789,812 | ||
nsv5953983 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 224,654,529 | 224,654,529 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17405671 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17405671 | Submitted genomic | NC_000002.12:g.223 789812_223789813in s252 | GRCh38 (hg38) | NC_000002.12 | Chr2 | 223,789,812 | 223,789,812 | ||
nssv17405671 | Remapped | Perfect | NC_000002.11:g.224 654529_224654530in s252 | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 224,654,529 | 224,654,529 |