nsv437052
- Organism: Homo sapiens
- Study:nstd17 (Conrad et al. 2005)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:227,580
- Publication(s):Conrad et al. 2005
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: 1064 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1064 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 2 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv437052 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 14,982,892 | 14,998,429 | 15,207,653 | 15,210,471 |
nsv437052 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 14,840,401 | 14,855,938 | 15,065,162 | 15,067,980 |
nsv437052 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000008.8 | Chr8 | 14,850,767 | 14,866,304 | 15,075,528 | 15,078,346 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv466933 | Remapped | Perfect | NC_000008.11:g.(14 982892_14998429)_( 15207653_15210471) del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 14,982,892 | 14,998,429 | 15,207,653 | 15,210,471 |
nssv466933 | Remapped | Perfect | NC_000008.10:g.(14 840401_14855938)_( 15065162_15067980) del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 14,840,401 | 14,855,938 | 15,065,162 | 15,067,980 |
nssv466933 | Submitted genomic | NC_000008.8:g.(148 50767_14866304)_(1 5075528_15078346)d el | NCBI34 (hg16) | NC_000008.8 | Chr8 | 14,850,767 | 14,866,304 | 15,075,528 | 15,078,346 |