nsv483065
- Organism: Homo sapiens
- Study:nstd41 (Iafrate et al. 2004)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:159,262
- Publication(s):Iafrate et al. 2004
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: 497 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 497 SVs from 50 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv483065 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 108,336,386 | 108,495,647 |
| nsv483065 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 110,096,144 | 110,255,405 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv2996381 | copy number gain | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2996381 | Remapped | Perfect | NC_000010.11:g.(?_ 108336386)_(108495 647_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 108,336,386 | 108,495,647 |
| nssv2996381 | Submitted genomic | NC_000010.10:g.(?_ 110096144)_(110255 405_?)dup | GRCh37 (hg19) | NC_000010.10 | Chr10 | 110,096,144 | 110,255,405 |