esv2574735
- Organism: Homo sapiens
- Study:estd197 (McKernan et al. 2009)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:30,727
- Description:originalFile=Yoruban_cnv.gff
- Publication(s):McKernan et al. 2009
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: 958 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 958 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 623 SVs from 29 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 |
---|---|---|---|---|---|---|---|---|---|
esv2574735 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 1,581,679 | 1,612,405 |
esv2574735 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 1,562,325 | 1,593,051 |
esv2574735 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 1,510,325 | 1,541,051 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv5293388 | Remapped | Perfect | NC_000020.11:g.(?_ 1581679)_(1612405_ ?)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 1,581,679 | 1,612,405 |
essv5293388 | Remapped | Perfect | NC_000020.10:g.(?_ 1562325)_(1593051_ ?)del | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 1,562,325 | 1,593,051 |
essv5293388 | Submitted genomic | NC_000020.9:g.(?_1 510325)_(1541051_? )del | NCBI36 (hg18) | NC_000020.9 | Chr20 | 1,510,325 | 1,541,051 |