nsv821655
- Organism: Homo sapiens
- Study:nstd66 (Sebat et al. 2004)
- Variant Type:copy number variation
- Method Type:ROMA
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,317,248
- Publication(s):Sebat 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: 6813 SVs from 119 studies. See in: genome view
Overlapping variant regions from other studies: 6813 SVs from 119 studies. See in: genome view
Overlapping variant regions from other studies: 665 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821655 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 3,766,075 | 5,083,322 |
| nsv821655 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 3,623,597 | 4,940,844 |
| nsv821655 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 3,611,005 | 4,928,252 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv1421201 | copy number gain | ROMA | Probe signal intensity |
| nssv1421203 | copy number gain | ROMA | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421201 | Remapped | Perfect | NC_000008.11:g.(?_ 3766075)_(5083322_ ?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 3,766,075 | 5,083,322 |
| nssv1421203 | Remapped | Perfect | NC_000008.11:g.(?_ 3766075)_(5083322_ ?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 3,766,075 | 5,083,322 |
| nssv1421201 | Remapped | Perfect | NC_000008.10:g.(?_ 3623597)_(4940844_ ?)dup | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 3,623,597 | 4,940,844 |
| nssv1421203 | Remapped | Perfect | NC_000008.10:g.(?_ 3623597)_(4940844_ ?)dup | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 3,623,597 | 4,940,844 |
| nssv1421201 | Submitted genomic | NC_000008.9:g.(?_3 611005)_(4928252_? )dup | NCBI35 (hg17) | NC_000008.9 | Chr8 | 3,611,005 | 4,928,252 | ||
| nssv1421203 | Submitted genomic | NC_000008.9:g.(?_3 611005)_(4928252_? )dup | NCBI35 (hg17) | NC_000008.9 | Chr8 | 3,611,005 | 4,928,252 |