nsv458104
- Organism: Homo sapiens
- Study:nstd27 (Itsara et al. 2009)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:364,602
- Publication(s):Itsara et al. 2009
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: 1709 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 1709 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 134 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv458104 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 66,174,053 | 66,538,654 |
| nsv458104 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 63,841,290 | 64,205,891 |
| nsv458104 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000018.8 | Chr18 | 61,992,270 | 62,356,871 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| nssv535139 | copy number loss | 1780854103_A | SNP array | SNP genotyping analysis | 1 | 10 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv535139 | Remapped | Perfect | NC_000018.10:g.(?_ 66174053)_(6653865 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 66,174,053 | 66,538,654 |
| nssv535139 | Remapped | Perfect | NC_000018.9:g.(?_6 3841290)_(64205891 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 63,841,290 | 64,205,891 |
| nssv535139 | Submitted genomic | NC_000018.8:g.(?_6 1992270)_(62356871 _?)del | NCBI35 (hg17) | NC_000018.8 | Chr18 | 61,992,270 | 62,356,871 |