nsv899243
- Organism: Homo sapiens
- Study:nstd71 (Xu et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:132,910
- Publication(s):Xu et al. 2011
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: 483 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 483 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 134 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv899243 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 71,240,332 | 71,260,539 | 71,354,510 | 71,373,241 |
| nsv899243 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 71,634,112 | 71,654,319 | 71,748,290 | 71,767,021 |
| nsv899243 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 69,920,379 | 69,940,586 | 70,034,557 | 70,053,288 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1567689 | Remapped | Perfect | NC_000012.12:g.(71 240332_71260539)_( 71354510_71373241) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 71,240,332 | 71,260,539 | 71,354,510 | 71,373,241 |
| nssv1589714 | Remapped | Perfect | NC_000012.12:g.(71 240332_71260539)_( 71354510_71373241) dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 71,240,332 | 71,260,539 | 71,354,510 | 71,373,241 |
| nssv1567689 | Remapped | Perfect | NC_000012.11:g.(71 634112_71654319)_( 71748290_71767021) del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 71,634,112 | 71,654,319 | 71,748,290 | 71,767,021 |
| nssv1589714 | Remapped | Perfect | NC_000012.11:g.(71 634112_71654319)_( 71748290_71767021) dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 71,634,112 | 71,654,319 | 71,748,290 | 71,767,021 |
| nssv1567689 | Submitted genomic | NC_000012.10:g.(69 920379_69940586)_( 70034557_70053288) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 69,920,379 | 69,940,586 | 70,034,557 | 70,053,288 | ||
| nssv1589714 | Submitted genomic | NC_000012.10:g.(69 920379_69940586)_( 70034557_70053288) dup | NCBI36 (hg18) | NC_000012.10 | Chr12 | 69,920,379 | 69,940,586 | 70,034,557 | 70,053,288 |