nsv832334
- Organism: Homo sapiens
- Study:nstd68 (Wong et al. 2006)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:249,788
- Publication(s):Wong et al. 2006
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: 788 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 789 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 28 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 | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv832334 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 13,915,799 | 14,165,586 |
nsv832334 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 14,068,733 | 14,318,520 |
nsv832334 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000012.9 | Chr12 | 13,960,000 | 14,209,787 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv1449686 | copy number gain | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1449686 | Remapped | Perfect | NC_000012.12:g.(13 915799_?)_(?_14165 586)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 13,915,799 | 14,165,586 |
nssv1449686 | Remapped | Perfect | NC_000012.11:g.(14 068733_?)_(?_14318 520)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 14,068,733 | 14,318,520 |
nssv1449686 | Submitted genomic | NC_000012.9:g.(139 60000_?)_(?_142097 87)dup | NCBI35 (hg17) | NC_000012.9 | Chr12 | 13,960,000 | 14,209,787 |