nsv817613
- Organism: Homo sapiens
- Study:nstd58 (Forsberg et al. 2012)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:103,248,007
- Publication(s):Forsberg et al. 2012
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: 290331 SVs from 156 studies. See in: genome view
Overlapping variant regions from other studies: 289406 SVs from 154 studies. See in: genome view
Overlapping variant regions from other studies: 84166 SVs from 47 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv817613 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 86,849,099 | 86,849,099 | 190,097,105 | 190,097,105 |
| nsv817613 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 87,770,252 | 87,770,252 | 190,828,225 | - |
| nsv817613 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 87,989,276 | 88,111,683 | 191,252,241 | 191,252,241 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv1415557 | complex substitution | 697 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|
| nssv1415557 | Remapped | Good | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 86,849,099 | 86,849,099 | 190,097,105 | 190,097,105 |
| nssv1415557 | Remapped | Good | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 87,770,252 | 87,770,252 | 190,828,225 | - |
| nssv1415557 | Submitted genomic | NCBI36 (hg18) | NC_000004.10 | Chr4 | 87,989,276 | 88,111,683 | 191,252,241 | 191,252,241 |