nsv821667
- Organism: Homo sapiens
- Study:nstd66 (Sebat et al. 2004)
- Variant Type:copy number variation
- Method Type:ROMA
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,765,645
- 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: 7536 SVs from 130 studies. See in: genome view
Overlapping variant regions from other studies: 3458 SVs from 108 studies. See in: genome view
Overlapping variant regions from other studies: 4433 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 517 SVs from 17 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 |
---|---|---|---|---|---|---|---|---|---|
nsv821667 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 46,157,935 | 47,923,579 |
nsv821667 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 47,006,954 | 47,531,169 |
nsv821667 | Remapped | Pass | GRCh37.p13 | PATCHES | First Pass | NW_003871068.1 | Chr10|NW_0 03871068.1 | 431,049 | 2,010,264 |
nsv821667 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 46,397,301 | 47,102,745 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv1421241 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv1421241 | Remapped | Pass | NC_000010.11:g.(?_ 46157935)_(4792357 9_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 46,157,935 | 47,923,579 |
nssv1421241 | Remapped | Pass | NW_003871068.1:g.( ?_431049)_(2010264 _?)dup | GRCh37.p13 | First Pass | NW_003871068.1 | Chr10|NW_0 03871068.1 | 431,049 | 2,010,264 |
nssv1421241 | Remapped | Pass | NC_000010.10:g.(?_ 47006954)_(4753116 9_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 47,006,954 | 47,531,169 |
nssv1421241 | Submitted genomic | NC_000010.8:g.(?_4 6397301)_(47102745 _?)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 46,397,301 | 47,102,745 |