nsv825432
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:99,043
- Publication(s):Park et al. 2010
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: 401 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 160 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 401 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 112 SVs from 18 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 |
---|---|---|---|---|---|---|---|---|---|
nsv825432 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 65,611,071 | 65,710,113 |
nsv825432 | Remapped | Pass | GRCh38.p12 | PATCHES | Second Pass | NW_013171806.1 | Chr10|NW_0 13171806.1 | 111,664 | 185,507 |
nsv825432 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 67,370,829 | 67,469,871 |
nsv825432 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 67,040,835 | 67,139,877 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1439064 | Remapped | Pass | NW_013171806.1:g.( ?_111664)_(185507_ ?)del | GRCh38.p12 | Second Pass | NW_013171806.1 | Chr10|NW_0 13171806.1 | 111,664 | 185,507 |
nssv1439064 | Remapped | Perfect | NC_000010.11:g.(?_ 65611071)_(6571011 3_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 65,611,071 | 65,710,113 |
nssv1439064 | Remapped | Perfect | NC_000010.10:g.(?_ 67370829)_(6746987 1_?)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 67,370,829 | 67,469,871 |
nssv1439064 | Submitted genomic | NC_000010.9:g.(?_6 7040835)_(67139877 _?)del | NCBI36 (hg18) | NC_000010.9 | Chr10 | 67,040,835 | 67,139,877 |