nsv482672
- Organism: Homo sapiens
- Study:nstd40 (Sharp et al. 2006)
- Variant Type:sequence alteration
- Method Type:BAC aCGH
- Submitted on:NCBI34 (hg16)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:97,396
- Publication(s):Sharp et al. 2006
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: 1100 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 1112 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 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 |
---|---|---|---|---|---|---|---|---|---|
nsv482672 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 97,157,497 | 97,254,892 |
nsv482672 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 97,823,234 | 97,920,629 |
nsv482672 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | GPC_000000200.1 | Chr2 | 97,307,990 | 97,456,304 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv3006331 | sequence alteration | BAC aCGH | Probe signal intensity |
nssv3008804 | sequence alteration | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv3006331 | Remapped | Pass | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,157,497 | 97,254,892 |
nssv3008804 | Remapped | Pass | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,157,497 | 97,254,892 |
nssv3006331 | Remapped | Pass | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 97,823,234 | 97,920,629 |
nssv3008804 | Remapped | Pass | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 97,823,234 | 97,920,629 |
nssv3006331 | Submitted genomic | NCBI34 (hg16) | GPC_000000200.1 | Chr2 | 97,307,990 | 97,456,304 | ||
nssv3008804 | Submitted genomic | NCBI34 (hg16) | GPC_000000200.1 | Chr2 | 97,307,990 | 97,456,304 |