nsv818667
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:63,911
- Publication(s):Wang et al. 2007
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: 568 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 568 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 27 SVs from 7 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 |
---|---|---|---|---|---|---|---|---|---|
nsv818667 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 189,748,529 | 189,812,439 |
nsv818667 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 189,717,659 | 189,781,569 |
nsv818667 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000001.8 | Chr1 | 186,449,316 | 186,513,226 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1416123 | Remapped | Perfect | NC_000001.11:g.(?_ 189748529)_(189812 439_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,748,529 | 189,812,439 |
nssv1416124 | Remapped | Perfect | NC_000001.11:g.(?_ 189748529)_(189812 439_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,748,529 | 189,812,439 |
nssv1416123 | Remapped | Perfect | NC_000001.10:g.(?_ 189717659)_(189781 569_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 189,717,659 | 189,781,569 |
nssv1416124 | Remapped | Perfect | NC_000001.10:g.(?_ 189717659)_(189781 569_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 189,717,659 | 189,781,569 |
nssv1416123 | Submitted genomic | NC_000001.8:g.(?_1 86449316)_(1865132 26_?)del | NCBI35 (hg17) | NC_000001.8 | Chr1 | 186,449,316 | 186,513,226 | ||
nssv1416124 | Submitted genomic | NC_000001.8:g.(?_1 86449316)_(1865132 26_?)del | NCBI35 (hg17) | NC_000001.8 | Chr1 | 186,449,316 | 186,513,226 |