nsv8521
- Organism: Homo sapiens
- Study:nstd4 (Perry et al. 2008)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:86,946
- Publication(s):Perry et al. 2008
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: 121 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 108 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 31 SVs from 10 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv8521 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 68,427,991 | 68,514,936 |
| nsv8521 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000009.11 | Chr9 | 71,042,907 | 71,129,852 |
| nsv8521 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871067.1 | Chr9|NW_00 3871067.1 | 207,439 | 294,384 |
| nsv8521 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000009.9 | Chr9 | 68,272,461 | 68,359,406 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv20961 | Remapped | Perfect | NC_000009.12:g.(68 427991_68431715)_( 68454875_68514936) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 68,427,991 | 68,431,715 | 68,454,875 | 68,514,936 |
| nssv20961 | Remapped | Perfect | NW_003871067.1:g.( 207439_211163)_(23 4323_294384)del | GRCh37.p13 | First Pass | NW_003871067.1 | Chr9|NW_00 3871067.1 | 207,439 | 211,163 | 234,323 | 294,384 |
| nssv20961 | Remapped | Perfect | NC_000009.11:g.(71 042907_71046631)_( 71069791_71129852) del | GRCh37.p13 | Second Pass | NC_000009.11 | Chr9 | 71,042,907 | 71,046,631 | 71,069,791 | 71,129,852 |
| nssv20961 | Submitted genomic | NC_000009.9:g.(682 72461_68276185)_(6 8299345_68359406)d el | NCBI35 (hg17) | NC_000009.9 | Chr9 | 68,272,461 | 68,276,185 | 68,299,345 | 68,359,406 |