nsv590331
- 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:8,242
- 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: 409 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 408 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 |
---|---|---|---|---|---|---|---|---|---|
nsv590331 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 52,996,726 | 53,004,967 |
nsv590331 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 53,030,742 | 53,038,983 |
nsv590331 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 53,005,782 | 53,014,023 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv963276 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv963276 | Remapped | Perfect | NC_000003.12:g.(?_ 52996726)_(5300496 7_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 52,996,726 | 53,004,967 |
nssv963276 | Remapped | Perfect | NC_000003.11:g.(?_ 53030742)_(5303898 3_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 53,030,742 | 53,038,983 |
nssv963276 | Submitted genomic | NC_000003.10:g.(?_ 53005782)_(5301402 3_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 53,005,782 | 53,014,023 |