nsv1014359
- Organism: Homo sapiens
- Study:nstd100 (Coe et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:144,412
- Publication(s):Coe et al. 2014
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: 793 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 793 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 322 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1014359 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 130,044,004 | 130,188,415 |
| nsv1014359 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 129,762,847 | 129,907,258 |
| nsv1014359 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 131,245,537 | 131,389,948 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3603893 | copy number gain | SNP array | Probe signal intensity |
| nssv3603894 | copy number gain | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3603893 | Remapped | Perfect | NC_000003.12:g.(?_ 130044004)_(130188 415_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 130,044,004 | 130,188,415 |
| nssv3603894 | Remapped | Perfect | NC_000003.12:g.(?_ 130044004)_(130188 415_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 130,044,004 | 130,188,415 |
| nssv3603893 | Remapped | Perfect | NC_000003.11:g.(?_ 129762847)_(129907 258_?)dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 129,762,847 | 129,907,258 |
| nssv3603894 | Remapped | Perfect | NC_000003.11:g.(?_ 129762847)_(129907 258_?)dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 129,762,847 | 129,907,258 |
| nssv3603893 | Submitted genomic | NC_000003.10:g.(?_ 131245537)_(131389 948_?)dup | NCBI36 (hg18) | NC_000003.10 | Chr3 | 131,245,537 | 131,389,948 | ||
| nssv3603894 | Submitted genomic | NC_000003.10:g.(?_ 131245537)_(131389 948_?)dup | NCBI36 (hg18) | NC_000003.10 | Chr3 | 131,245,537 | 131,389,948 |