nsv475605
- Organism: Homo sapiens
- Study:nstd35 (Kidd et al. 2010)
- Variant Type:complex substitution
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:104
- Description:complex allele - no allele length provided
- Publication(s):Kidd et al. 2010
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: 207 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 30 SVs from 12 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 19 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv475605 | Remapped | Pass | GRCh37.p13 | Primary Assembly | Second Pass | NC_000017.10 | Chr17 | 79,498,344 | 79,498,447 |
| nsv475605 | Remapped | Pass | GRCh37.p13 | PATCHES | First Pass | NW_003871087.1 | Chr17|NW_0 03871087.1 | 185,956 | 186,059 |
| nsv475605 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 77,112,939 | 77,113,072 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3016755 | Remapped | Pass | GRCh37.p13 | First Pass | NW_003871087.1 | Chr17|NW_0 03871087.1 | 185,956 | 186,059 |
| nssv3016755 | Remapped | Pass | GRCh37.p13 | Second Pass | NC_000017.10 | Chr17 | 79,498,344 | 79,498,447 |
| nssv3016755 | Submitted genomic | NCBI36 (hg18) | NC_000017.9 | Chr17 | 77,112,939 | 77,113,072 |