esv3584856
- Organism: Homo sapiens
- Study:estd213 (Mokhtar et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:36,474
- Publication(s):Mokhtar 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: 355 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 355 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 158 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 |
---|---|---|---|---|---|---|---|---|---|
esv3584856 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 160,611,057 | 160,647,530 |
esv3584856 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 161,032,089 | 161,068,562 |
esv3584856 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 160,952,079 | 160,988,552 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv9838590 | Remapped | Perfect | NC_000006.12:g.(?_ 160611057)_(160647 530_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,611,057 | 160,647,530 |
essv9838591 | Remapped | Perfect | NC_000006.12:g.(?_ 160611057)_(160647 530_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 160,611,057 | 160,647,530 |
essv9838590 | Remapped | Perfect | NC_000006.11:g.(?_ 161032089)_(161068 562_?)del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 161,032,089 | 161,068,562 |
essv9838591 | Remapped | Perfect | NC_000006.11:g.(?_ 161032089)_(161068 562_?)del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 161,032,089 | 161,068,562 |
essv9838590 | Submitted genomic | NC_000006.10:g.(?_ 160952079)_(160988 552_?)del | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,952,079 | 160,988,552 | ||
essv9838591 | Submitted genomic | NC_000006.10:g.(?_ 160952079)_(160988 552_?)del | NCBI36 (hg18) | NC_000006.10 | Chr6 | 160,952,079 | 160,988,552 |