nsv949476
- Organism: Homo sapiens
- Study:nstd85 (vanSilfhout et al. 2013)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:336,913
- Publication(s):Vulto-van Silfhout et al. 2013
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: 1132 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 1132 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 37 SVs from 5 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 |
---|---|---|---|---|---|---|---|---|---|
nsv949476 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 133,007,775 | 133,344,687 |
nsv949476 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 132,877,670 | 133,214,582 |
nsv949476 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 132,382,880 | 132,719,792 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|---|---|---|---|
nssv2768167 | copy number gain | SNP array | SNP genotyping analysis | 4 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv2768167 | Remapped | Perfect | NC_000011.10:g.(?_ 133007775)_(133344 687_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 133,007,775 | 133,344,687 |
nssv2768167 | Remapped | Perfect | NC_000011.9:g.(?_1 32877670)_(1332145 82_?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 132,877,670 | 133,214,582 |
nssv2768167 | Submitted genomic | NC_000011.8:g.(?_1 32382880)_(1327197 92_?)dup | NCBI35 (hg17) | NC_000011.8 | Chr11 | 132,382,880 | 132,719,792 |