nsv3964569
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:complex substitution
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:56,702
- 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: 331 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 331 SVs from 48 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3964569 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 72,829,481 | 72,886,182 | ||
nsv3964569 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 70,825,620 | 70,882,321 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15221299 | complex substitution | Optical mapping | Optical mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|
nssv15221299 | Submitted genomic | GRCh38 (hg38) | NC_000017.11 | Chr17 | 72,829,481 | 72,886,182 | ||
nssv15221299 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 70,825,620 | 70,882,321 |