nsv437530
- Organism: Homo sapiens
- Study:nstd17 (Conrad et al. 2005)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:61,709
- Publication(s):Conrad et al. 2005
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: 590 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 590 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv437530 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 3,343,971 | 3,352,894 | 3,401,692 | 3,405,679 |
| nsv437530 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 3,383,603 | 3,392,526 | 3,441,324 | 3,445,311 |
| nsv437530 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000007.10 | Chr7 | 3,127,941 | 3,136,864 | 3,185,662 | 3,189,649 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv467411 | Remapped | Perfect | NC_000007.14:g.(33 43971_3352894)_(34 01692_3405679)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 3,343,971 | 3,352,894 | 3,401,692 | 3,405,679 |
| nssv467411 | Remapped | Perfect | NC_000007.13:g.(33 83603_3392526)_(34 41324_3445311)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 3,383,603 | 3,392,526 | 3,441,324 | 3,445,311 |
| nssv467411 | Submitted genomic | NC_000007.10:g.(31 27941_3136864)_(31 85662_3189649)del | NCBI34 (hg16) | NC_000007.10 | Chr7 | 3,127,941 | 3,136,864 | 3,185,662 | 3,189,649 |