esv2422454
- Organism: Homo sapiens
- Study:estd196 (Simon-Sanchez et al. 2006)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:106,904
- Publication(s):Simon-Sanchez et al. 2006
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: 888 SVs from 104 studies. See in: genome view
Overlapping variant regions from other studies: 888 SVs from 104 studies. See in: genome view
Overlapping variant regions from other studies: 57 SVs from 14 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 |
---|---|---|---|---|---|---|---|---|---|
esv2422454 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 22,594,557 | 22,701,460 |
esv2422454 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 22,605,878 | 22,712,781 |
esv2422454 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000016.8 | Chr16 | 22,513,379 | 22,620,282 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis |
---|---|---|---|---|
essv5161524 | deletion | ND03971 | 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 |
---|---|---|---|---|---|---|---|---|---|
essv5161524 | Remapped | Perfect | NC_000016.10:g.(?_ 22594557)_(2270146 0_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 22,594,557 | 22,701,460 |
essv5161524 | Remapped | Perfect | NC_000016.9:g.(?_2 2605878)_(22712781 _?)del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 22,605,878 | 22,712,781 |
essv5161524 | Submitted genomic | NC_000016.8:g.(?_2 2513379)_(22620282 _?)del | NCBI35 (hg17) | NC_000016.8 | Chr16 | 22,513,379 | 22,620,282 |