nsv1568
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:56,757
- Publication(s):Kidd et al. 2008
- TRACE: TEMPLATE_ID='1200277_ABC11_2_1_000048376900_G23'
- TRACE: TEMPLATE_ID='1200277_ABC11_2_1_000048377000_L12'
- TRACE: TEMPLATE_ID='171515_ABC9_3_5_000043920200_J19'
- TRACE: TEMPLATE_ID='171515_ABC9_3_5_000043946000_A12'
- TRACE: TEMPLATE_ID='172343_ABC9_3_5_000043979000_G23'
- Overlapping Genes
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: 203 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 203 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 10 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1568 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 63,996,338 | 64,053,094 |
| nsv1568 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 64,288,537 | 64,345,293 |
| nsv1568 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 62,075,590 | 62,132,346 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv10057 | Remapped | Perfect | NC_000015.10:g.(63 996338_?)_(?_64027 819)ins8023 | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 63,996,338 | 64,027,819 |
| nssv2939 | Remapped | Perfect | NC_000015.10:g.(64 019242_?)_(?_64053 094)ins6176 | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 64,019,242 | 64,053,094 |
| nssv10057 | Remapped | Perfect | NC_000015.9:g.(642 88537_?)_(?_643200 18)ins8023 | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 64,288,537 | 64,320,018 |
| nssv2939 | Remapped | Perfect | NC_000015.9:g.(643 11441_?)_(?_643452 93)ins6176 | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 64,311,441 | 64,345,293 |
| nssv10057 | Submitted genomic | NC_000015.8:g.(620 75590_?)_(?_621070 71)ins8023 | NCBI35 (hg17) | NC_000015.8 | Chr15 | 62,075,590 | 62,107,071 | ||
| nssv2939 | Submitted genomic | NC_000015.8:g.(620 98494_?)_(?_621323 46)ins6176 | NCBI35 (hg17) | NC_000015.8 | Chr15 | 62,098,494 | 62,132,346 |