esv34111
- Organism: Homo sapiens
- Study:estd49 (Gusev et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:288,106
- Publication(s):Gusev et al. 2008
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: 1258 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1258 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 442 SVs from 22 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 |
---|---|---|---|---|---|---|---|---|---|
esv34111 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 24,781,123 | 25,069,228 |
esv34111 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 24,802,669 | 25,090,774 |
esv34111 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 24,759,245 | 25,047,350 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
essv6990598 | copy number loss | SNP array | SNP genotyping analysis |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv6990598 | Remapped | Perfect | NC_000011.10:g.(?_ 24781123)_(2506922 8_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 24,781,123 | 25,069,228 |
essv6990598 | Remapped | Perfect | NC_000011.9:g.(?_2 4802669)_(25090774 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 24,802,669 | 25,090,774 |
essv6990598 | Submitted genomic | NC_000011.8:g.(?_2 4759245)_(25047350 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 24,759,245 | 25,047,350 |