nsv436985
- Organism: Homo sapiens
- Study:nstd17 (Conrad et al. 2005)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:108,529
- Publication(s):Conrad et al. 2005
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: 973 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 973 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 2 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv436985 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 105,089,919 | 105,105,485 | 105,124,459 | 105,198,447 |
nsv436985 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 104,425,620 | 104,441,186 | 104,460,160 | 104,534,148 |
nsv436985 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000005.7 | Chr5 | 104,501,836 | 104,517,402 | 104,536,376 | 104,610,364 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv466866 | Remapped | Perfect | NC_000005.10:g.(10 5089919_105105485) _(105124459_105198 447)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 105,089,919 | 105,105,485 | 105,124,459 | 105,198,447 |
nssv466866 | Remapped | Perfect | NC_000005.9:g.(104 425620_104441186)_ (104460160_1045341 48)del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 104,425,620 | 104,441,186 | 104,460,160 | 104,534,148 |
nssv466866 | Submitted genomic | NC_000005.7:g.(104 501836_104517402)_ (104536376_1046103 64)del | NCBI34 (hg16) | NC_000005.7 | Chr5 | 104,501,836 | 104,517,402 | 104,536,376 | 104,610,364 |