nsv1125883
- Organism: Homo sapiens
- Study:nstd106 (Alsmadi et al. 2014)
- Variant Type:tandem duplication
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:27,899
- Publication(s):Alsmadi et al. 2014
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: 176 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 176 SVs from 41 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 |
---|---|---|---|---|---|---|---|---|---|
nsv1125883 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 96,193,439 | 96,221,337 |
nsv1125883 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 96,641,315 | 96,669,213 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv3963399 | Remapped | Perfect | NC_000006.12:g.(96 193439_?)_(?_96221 337)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 96,193,439 | 96,221,337 |
nssv3979920 | Remapped | Perfect | NC_000006.12:g.(96 193439_?)_(?_96221 337)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 96,193,439 | 96,221,337 |
nssv3963399 | Submitted genomic | NC_000006.11:g.(96 641315_?)_(?_96669 213)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 96,641,315 | 96,669,213 | ||
nssv3979920 | Submitted genomic | NC_000006.11:g.(96 641315_?)_(?_96669 213)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 96,641,315 | 96,669,213 |