nsv735
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:83,485
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 367 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 367 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 20 SVs from 5 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 |
---|---|---|---|---|---|---|---|---|---|
nsv735 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 59,405,451 | 59,488,935 |
nsv735 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 59,799,232 | 59,882,716 |
nsv735 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000012.9 | Chr12 | 58,085,499 | 58,168,983 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv9034 | Remapped | Perfect | NC_000012.12:g.(59 405451_?)_(?_59446 060)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 59,405,451 | 59,446,060 |
nssv6511 | Remapped | Perfect | NC_000012.12:g.(59 443306_?)_(?_59488 935)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 59,443,306 | 59,488,935 |
nssv9034 | Remapped | Perfect | NC_000012.11:g.(59 799232_?)_(?_59839 841)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 59,799,232 | 59,839,841 |
nssv6511 | Remapped | Perfect | NC_000012.11:g.(59 837087_?)_(?_59882 716)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 59,837,087 | 59,882,716 |
nssv9034 | Submitted genomic | NC_000012.9:g.(580 85499_?)_(?_581261 08)del5974 | NCBI35 (hg17) | NC_000012.9 | Chr12 | 58,085,499 | 58,126,108 | ||
nssv6511 | Submitted genomic | NC_000012.9:g.(581 23354_?)_(?_581689 83)del6200 | NCBI35 (hg17) | NC_000012.9 | Chr12 | 58,123,354 | 58,168,983 |