nsv508
- 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:63,952
- Publication(s):Kidd et al. 2008
- TRACE: TEMPLATE_ID='1209408_ABC14_4_1_000050190100_I1'
- TRACE: TEMPLATE_ID='1209408_ABC14_4_1_000051454500_A11'
- TRACE: TEMPLATE_ID='174552_ABC10_2_1_000001583770_J12'
- TRACE: TEMPLATE_ID='174552_ABC10_2_1_000001607470_L19'
- TRACE: TEMPLATE_ID='174552_ABC10_2_1_000044688600_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: 230 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 230 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 16 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv508 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 117,579,088 | 117,643,039 |
| nsv508 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 117,449,803 | 117,513,754 |
| nsv508 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000011.8 | Chr11 | 116,955,013 | 117,018,964 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1043 | Remapped | Perfect | NC_000011.10:g.(11 7579088_?)_(?_1176 14363)ins5725 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 117,579,088 | 117,614,363 |
| nssv8965 | Remapped | Perfect | NC_000011.10:g.(11 7609146_?)_(?_1176 43039)ins5546 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 117,609,146 | 117,643,039 |
| nssv1043 | Remapped | Perfect | NC_000011.9:g.(117 449803_?)_(?_11748 5078)ins5725 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 117,449,803 | 117,485,078 |
| nssv8965 | Remapped | Perfect | NC_000011.9:g.(117 479861_?)_(?_11751 3754)ins5546 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 117,479,861 | 117,513,754 |
| nssv1043 | Submitted genomic | NC_000011.8:g.(116 955013_?)_(?_11699 0288)ins5725 | NCBI35 (hg17) | NC_000011.8 | Chr11 | 116,955,013 | 116,990,288 | ||
| nssv8965 | Submitted genomic | NC_000011.8:g.(116 985071_?)_(?_11701 8964)ins5546 | NCBI35 (hg17) | NC_000011.8 | Chr11 | 116,985,071 | 117,018,964 |