nsv2733261
- Organism: Homo sapiens
- Study:nstd130 (Leppa et al. 2016)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:8,575,340
- Publication(s):Leppa et al. 2016
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: 21641 SVs from 128 studies. See in: genome view
Overlapping variant regions from other studies: 21648 SVs from 128 studies. See in: genome view
Overlapping variant regions from other studies: 6445 SVs from 36 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 |
---|---|---|---|---|---|---|---|---|---|
nsv2733261 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 103,514,470 | 112,089,809 |
nsv2733261 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 103,385,198 | 111,960,533 |
nsv2733261 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 102,890,408 | 111,465,743 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv13591705 | deletion | SNP array | Probe signal intensity |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv13591705 | Remapped | Perfect | NC_000011.10:g.(?_ 103514470)_(112089 809_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 103,514,470 | 112,089,809 |
nssv13591705 | Remapped | Perfect | NC_000011.9:g.(?_1 03385198)_(1119605 33_?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 103,385,198 | 111,960,533 |
nssv13591705 | Submitted genomic | NC_000011.8:g.(?_1 02890408)_(1114657 43_?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 102,890,408 | 111,465,743 |