nsv442230
- Organism: Homo sapiens
- Study:nstd22 (McCarroll et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:52,888
- Publication(s):McCarroll et al. 2008
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: 237 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 237 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 11 SVs from 6 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 |
---|---|---|---|---|---|---|---|---|---|
nsv442230 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 49,286,252 | 49,339,139 |
nsv442230 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 49,307,804 | 49,360,691 |
nsv442230 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 49,264,380 | 49,317,267 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1659296 | Remapped | Perfect | NC_000011.10:g.(?_ 49286252)_(4933913 9_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 49,286,252 | 49,339,139 |
nssv1659297 | Remapped | Perfect | NC_000011.10:g.(?_ 49286252)_(4933913 9_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 49,286,252 | 49,339,139 |
nssv1659298 | Remapped | Perfect | NC_000011.10:g.(?_ 49286252)_(4933913 9_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 49,286,252 | 49,339,139 |
nssv1659296 | Remapped | Perfect | NC_000011.9:g.(?_4 9307804)_(49360691 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 49,307,804 | 49,360,691 |
nssv1659297 | Remapped | Perfect | NC_000011.9:g.(?_4 9307804)_(49360691 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 49,307,804 | 49,360,691 |
nssv1659298 | Remapped | Perfect | NC_000011.9:g.(?_4 9307804)_(49360691 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 49,307,804 | 49,360,691 |
nssv1659296 | Submitted genomic | NC_000011.8:g.(?_4 9264380)_(49317267 _?)del | NCBI35 (hg17) | NC_000011.8 | Chr11 | 49,264,380 | 49,317,267 | ||
nssv1659297 | Submitted genomic | NC_000011.8:g.(?_4 9264380)_(49317267 _?)del | NCBI35 (hg17) | NC_000011.8 | Chr11 | 49,264,380 | 49,317,267 | ||
nssv1659298 | Submitted genomic | NC_000011.8:g.(?_4 9264380)_(49317267 _?)del | NCBI35 (hg17) | NC_000011.8 | Chr11 | 49,264,380 | 49,317,267 |