nsv483079
- 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:177,094
- 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: 798 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 798 SVs from 75 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv483079 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 11,070,537 | 11,247,630 |
| nsv483079 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 11,070,649 | 11,247,742 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv2995910 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv2995910 | Remapped | Perfect | NC_000005.10:g.(?_ 11070537)_(1124763 0_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 11,070,537 | 11,247,630 |
| nssv2995910 | Submitted genomic | NC_000005.9:g.(?_1 1070649)_(11247742 _?)dup | GRCh37 (hg19) | NC_000005.9 | Chr5 | 11,070,649 | 11,247,742 |