nsv984789
- Organism: Homo sapiens
- Study:nstd92 (Forsberg et al. 2014)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:12,763,864
- Publication(s):Forsberg et al. 2014
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: 55301 SVs from 140 studies. See in: genome view
Overlapping variant regions from other studies: 54048 SVs from 140 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nsv984789 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 94,115,593 | 106,879,456 |
nsv984789 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 94,156,220 | 107,287,663 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv3217437 | complex substitution | PIVUS931 | SNP array | SNP genotyping analysis | nssv3217438 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|
nssv3217437 | Remapped | Good | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 94,115,593 | 106,879,456 |
nssv3217437 | Submitted genomic | GRCh37 (hg19) | NC_000014.8 | Chr14 | 94,156,220 | 107,287,663 |