nsv817836
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:30,482
- Publication(s):Wang et al. 2007
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: 1068 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1068 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 22 SVs from 11 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 |
---|---|---|---|---|---|---|---|---|---|
nsv817836 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 40,827,379 | 40,857,860 |
nsv817836 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 41,333,284 | 41,363,765 |
nsv817836 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000019.8 | Chr19 | 46,025,124 | 46,055,605 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1416690 | Remapped | Perfect | NC_000019.10:g.(?_ 40827379)_(4085786 0_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 40,827,379 | 40,857,860 |
nssv1416691 | Remapped | Perfect | NC_000019.10:g.(?_ 40827379)_(4085786 0_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 40,827,379 | 40,857,860 |
nssv1416692 | Remapped | Perfect | NC_000019.10:g.(?_ 40827379)_(4085786 0_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 40,827,379 | 40,857,860 |
nssv1416690 | Remapped | Perfect | NC_000019.9:g.(?_4 1333284)_(41363765 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 41,333,284 | 41,363,765 |
nssv1416691 | Remapped | Perfect | NC_000019.9:g.(?_4 1333284)_(41363765 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 41,333,284 | 41,363,765 |
nssv1416692 | Remapped | Perfect | NC_000019.9:g.(?_4 1333284)_(41363765 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 41,333,284 | 41,363,765 |
nssv1416690 | Submitted genomic | NC_000019.8:g.(?_4 6025124)_(46055605 _?)del | NCBI35 (hg17) | NC_000019.8 | Chr19 | 46,025,124 | 46,055,605 | ||
nssv1416691 | Submitted genomic | NC_000019.8:g.(?_4 6025124)_(46055605 _?)dup | NCBI35 (hg17) | NC_000019.8 | Chr19 | 46,025,124 | 46,055,605 | ||
nssv1416692 | Submitted genomic | NC_000019.8:g.(?_4 6025124)_(46055605 _?)del | NCBI35 (hg17) | NC_000019.8 | Chr19 | 46,025,124 | 46,055,605 |