esv2527591
- 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:41,235
- 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: 2181 SVs from 87 studies. See in: genome view
Overlapping variant regions from other studies: 2183 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 1568 SVs from 28 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 |
---|---|---|---|---|---|---|---|---|---|
esv2527591 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 32,475,759 | 32,516,993 |
esv2527591 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 32,487,080 | 32,528,314 |
esv2527591 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 32,394,581 | 32,435,815 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv5281870 | Remapped | Perfect | NC_000016.10:g.(?_ 32475759)_(3251699 3_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 32,475,759 | 32,516,993 |
essv5281870 | Remapped | Perfect | NC_000016.9:g.(?_3 2487080)_(32528314 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 32,487,080 | 32,528,314 |
essv5281870 | Submitted genomic | NC_000016.8:g.(?_3 2394581)_(32435815 _?)dup | NCBI36 (hg18) | NC_000016.8 | Chr16 | 32,394,581 | 32,435,815 |