esv995713
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:41,308
- Publication(s):Pang et al. 2010
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: 361 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 359 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 99 SVs from 19 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 |
---|---|---|---|---|---|---|---|---|---|
esv995713 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 47,554,844 | 47,596,151 |
esv995713 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 45,632,210 | 45,673,517 |
esv995713 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 42,987,209 | 43,028,516 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv3586258 | Remapped | Perfect | NC_000017.11:g.(?_ 47554844)_(4759615 1_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 47,554,844 | 47,596,151 |
essv3586258 | Remapped | Perfect | NC_000017.10:g.(?_ 45632210)_(4567351 7_?)dup | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 45,632,210 | 45,673,517 |
essv3586258 | Submitted genomic | NC_000017.9:g.(?_4 2987209)_(43028516 _?)dup | NCBI36 (hg18) | NC_000017.9 | Chr17 | 42,987,209 | 43,028,516 |