nsv569810
- Organism: Homo sapiens
- Study:nstd54 (Cooper et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:14,581
- Publication(s):Cooper 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: 148 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 41 SVs from 12 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 |
---|---|---|---|---|---|---|---|---|---|
nsv569810 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 69,214,001 | 69,228,581 |
nsv569810 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 69,506,340 | 69,520,920 |
nsv569810 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 67,293,394 | 67,307,974 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv844369 | copy number gain | SNP array | SNP genotyping analysis |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv844369 | Remapped | Perfect | NC_000015.10:g.(?_ 69214001)_(6922858 1_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 69,214,001 | 69,228,581 |
nssv844369 | Remapped | Perfect | NC_000015.9:g.(?_6 9506340)_(69520920 _?)dup | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 69,506,340 | 69,520,920 |
nssv844369 | Submitted genomic | NC_000015.8:g.(?_6 7293394)_(67307974 _?)dup | NCBI36 (hg18) | NC_000015.8 | Chr15 | 67,293,394 | 67,307,974 |