nsv1194190
- Organism: Homo sapiens
- Study:nstd113 (Polyak et al. 2015)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:5
- Validation:Not tested
- Clinical Assertions: No
- Region Size:73,589
- Publication(s):Polyak et al. 2015
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: 260 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 260 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 81 SVs from 19 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 |
---|---|---|---|---|---|---|---|---|---|
nsv1194190 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 106,235,552 | 106,309,140 |
nsv1194190 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 105,875,998 | 105,949,586 |
nsv1194190 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 105,663,234 | 105,736,822 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv7461685 | copy number loss | 26768 | Oligo aCGH | Probe signal intensity | nssv7473739, nssv7467353 |
nssv7466181 | copy number loss | 19688 | Oligo aCGH | Probe signal intensity | nssv7460918 |
nssv7468777 | copy number loss | 13214 | Oligo aCGH | Probe signal intensity | nssv7463112, nssv7460495, nssv7469782 |
nssv7473467 | copy number loss | 30765 | Oligo aCGH | Probe signal intensity | nssv7472192, nssv7473637, nssv7461463 |
nssv7474945 | copy number loss | 31961 | Oligo aCGH | Probe signal intensity | nssv7460177 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv7461685 | Remapped | Perfect | NC_000007.14:g.(?_ 106235552)_(106309 140_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 106,235,552 | 106,309,140 |
nssv7466181 | Remapped | Perfect | NC_000007.14:g.(?_ 106235552)_(106309 140_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 106,235,552 | 106,309,140 |
nssv7468777 | Remapped | Perfect | NC_000007.14:g.(?_ 106235552)_(106309 140_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 106,235,552 | 106,309,140 |
nssv7473467 | Remapped | Perfect | NC_000007.14:g.(?_ 106235552)_(106309 140_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 106,235,552 | 106,309,140 |
nssv7474945 | Remapped | Perfect | NC_000007.14:g.(?_ 106235552)_(106309 140_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 106,235,552 | 106,309,140 |
nssv7461685 | Remapped | Perfect | NC_000007.13:g.(?_ 105875998)_(105949 586_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 105,875,998 | 105,949,586 |
nssv7466181 | Remapped | Perfect | NC_000007.13:g.(?_ 105875998)_(105949 586_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 105,875,998 | 105,949,586 |
nssv7468777 | Remapped | Perfect | NC_000007.13:g.(?_ 105875998)_(105949 586_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 105,875,998 | 105,949,586 |
nssv7473467 | Remapped | Perfect | NC_000007.13:g.(?_ 105875998)_(105949 586_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 105,875,998 | 105,949,586 |
nssv7474945 | Remapped | Perfect | NC_000007.13:g.(?_ 105875998)_(105949 586_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 105,875,998 | 105,949,586 |
nssv7461685 | Submitted genomic | NC_000007.12:g.(?_ 105663234)_(105736 822_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 105,663,234 | 105,736,822 | ||
nssv7466181 | Submitted genomic | NC_000007.12:g.(?_ 105663234)_(105736 822_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 105,663,234 | 105,736,822 | ||
nssv7468777 | Submitted genomic | NC_000007.12:g.(?_ 105663234)_(105736 822_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 105,663,234 | 105,736,822 | ||
nssv7473467 | Submitted genomic | NC_000007.12:g.(?_ 105663234)_(105736 822_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 105,663,234 | 105,736,822 | ||
nssv7474945 | Submitted genomic | NC_000007.12:g.(?_ 105663234)_(105736 822_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 105,663,234 | 105,736,822 |