nsv3169850
- Organism: Homo sapiens
- Study:nstd156 (Fu et al. 2018)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:122,787
- Publication(s):Fu et al. 2018
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: 1326 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1326 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 547 SVs from 26 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv3169850 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 134,483,002 | 134,486,015 | 134,602,316 | 134,605,788 |
nsv3169850 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 134,352,896 | 134,355,909 | 134,472,210 | 134,475,682 |
nsv3169850 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 133,858,106 | 133,861,119 | 133,977,420 | 133,980,892 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv14244950 | Remapped | Perfect | NC_000011.10:g.(13 4483002_134486015) _(134596762_134597 591)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 134,483,002 | 134,486,015 | 134,596,762 | 134,597,591 |
nssv14249888 | Remapped | Perfect | NC_000011.10:g.(13 4483002_134486015) _(134602316_134605 788)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 134,483,002 | 134,486,015 | 134,602,316 | 134,605,788 |
nssv14244950 | Remapped | Perfect | NC_000011.9:g.(134 352896_134355909)_ (134466656_1344674 85)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 134,352,896 | 134,355,909 | 134,466,656 | 134,467,485 |
nssv14249888 | Remapped | Perfect | NC_000011.9:g.(134 352896_134355909)_ (134472210_1344756 82)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 134,352,896 | 134,355,909 | 134,472,210 | 134,475,682 |
nssv14244950 | Submitted genomic | NC_000011.8:g.(133 858106_133861119)_ (133971866_1339726 95)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 133,858,106 | 133,861,119 | 133,971,866 | 133,972,695 | ||
nssv14249888 | Submitted genomic | NC_000011.8:g.(133 858106_133861119)_ (133977420_1339808 92)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 133,858,106 | 133,861,119 | 133,977,420 | 133,980,892 |