nsv590329
- 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:8,487
- 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: 404 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 403 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 181 SVs from 24 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 |
---|---|---|---|---|---|---|---|---|---|
nsv590329 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 52,995,193 | 53,003,679 |
nsv590329 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 53,029,209 | 53,037,695 |
nsv590329 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 53,004,249 | 53,012,735 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv963274 | copy number loss | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv963274 | Remapped | Perfect | NC_000003.12:g.(?_ 52995193)_(5300367 9_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 52,995,193 | 53,003,679 |
nssv963274 | Remapped | Perfect | NC_000003.11:g.(?_ 53029209)_(5303769 5_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 53,029,209 | 53,037,695 |
nssv963274 | Submitted genomic | NC_000003.10:g.(?_ 53004249)_(5301273 5_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 53,004,249 | 53,012,735 |