nsv513747
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:5,784
- Publication(s):Arlt et al. 2011
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: 350 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 350 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 197 SVs from 16 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 |
---|---|---|---|---|---|---|---|---|---|
nsv513747 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 132,054,369 | 132,060,152 |
nsv513747 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 131,924,263 | 131,930,046 |
nsv513747 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 131,429,473 | 131,435,256 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv626999 | insertion | 1 | Sequencing | Paired-end mapping | 2,637 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv626999 | Remapped | Perfect | NC_000011.10:g.(13 2054369_?)_(?_1320 60152)ins5784 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 132,054,369 | 132,060,152 |
nssv626999 | Remapped | Perfect | NC_000011.9:g.(131 924263_?)_(?_13193 0046)ins5784 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 131,924,263 | 131,930,046 |
nssv626999 | Submitted genomic | NC_000011.8:g.(131 429473_?)_(?_13143 5256)ins5784 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 131,429,473 | 131,435,256 |