nsv442060
- Organism: Homo sapiens
- Study:nstd22 (McCarroll et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:41,587
- Publication(s):McCarroll 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: 210 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 210 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 6 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 | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nsv442060 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 108,955,958 | 108,997,544 |
nsv442060 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 108,596,015 | 108,637,601 |
nsv442060 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000007.11 | Chr7 | 108,189,966 | 108,231,552 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1658431 | Remapped | Perfect | NC_000007.14:g.(?_ 108955958)_(108997 544_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 108,955,958 | 108,997,544 |
nssv1658432 | Remapped | Perfect | NC_000007.14:g.(?_ 108955958)_(108997 544_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 108,955,958 | 108,997,544 |
nssv1658433 | Remapped | Perfect | NC_000007.14:g.(?_ 108955958)_(108997 544_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 108,955,958 | 108,997,544 |
nssv1658431 | Remapped | Perfect | NC_000007.13:g.(?_ 108596015)_(108637 601_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 108,596,015 | 108,637,601 |
nssv1658432 | Remapped | Perfect | NC_000007.13:g.(?_ 108596015)_(108637 601_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 108,596,015 | 108,637,601 |
nssv1658433 | Remapped | Perfect | NC_000007.13:g.(?_ 108596015)_(108637 601_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 108,596,015 | 108,637,601 |
nssv1658431 | Submitted genomic | NC_000007.11:g.(?_ 108189966)_(108231 552_?)dup | NCBI35 (hg17) | NC_000007.11 | Chr7 | 108,189,966 | 108,231,552 | ||
nssv1658432 | Submitted genomic | NC_000007.11:g.(?_ 108189966)_(108231 552_?)dup | NCBI35 (hg17) | NC_000007.11 | Chr7 | 108,189,966 | 108,231,552 | ||
nssv1658433 | Submitted genomic | NC_000007.11:g.(?_ 108189966)_(108231 552_?)dup | NCBI35 (hg17) | NC_000007.11 | Chr7 | 108,189,966 | 108,231,552 |