esv2756980
- Organism: Homo sapiens
- Study:estd1 (Redon 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:170,979
- Publication(s):Redon 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: 601 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 601 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 35 SVs from 9 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 |
---|---|---|---|---|---|---|---|---|---|
esv2756980 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 21,164,178 | 21,335,156 |
esv2756980 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 21,205,670 | 21,376,648 |
esv2756980 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000003.9 | Chr3 | 21,180,674 | 21,351,652 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
essv19877 | Remapped | Perfect | NC_000003.12:g.(21 164178_21223278)_( 21302104_21335156) dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 21,164,178 | 21,223,278 | 21,302,104 | 21,335,156 |
essv19877 | Remapped | Perfect | NC_000003.11:g.(21 205670_21264770)_( 21343596_21376648) dup | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 21,205,670 | 21,264,770 | 21,343,596 | 21,376,648 |
essv19877 | Submitted genomic | NC_000003.9:g.(211 80674_21239774)_(2 1318600_21351652)d up | NCBI35 (hg17) | NC_000003.9 | Chr3 | 21,180,674 | 21,239,774 | 21,318,600 | 21,351,652 |