esv2761105
- Organism: Homo sapiens
- Study:estd203 (Vogler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:182,137
- Publication(s):Vogler 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: 665 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 665 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 170 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 | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
esv2761105 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 126,179,485 | 126,361,621 |
esv2761105 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 125,819,539 | 126,001,675 |
esv2761105 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 125,606,775 | 125,788,911 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv7015017 | Remapped | Perfect | NC_000007.14:g.(?_ 126179485)_(126361 621_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 126,179,485 | 126,361,621 |
essv7015018 | Remapped | Perfect | NC_000007.14:g.(?_ 126179485)_(126361 621_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 126,179,485 | 126,361,621 |
essv7015017 | Remapped | Perfect | NC_000007.13:g.(?_ 125819539)_(126001 675_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 125,819,539 | 126,001,675 |
essv7015018 | Remapped | Perfect | NC_000007.13:g.(?_ 125819539)_(126001 675_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 125,819,539 | 126,001,675 |
essv7015017 | Submitted genomic | NC_000007.12:g.(?_ 125606775)_(125788 911_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 125,606,775 | 125,788,911 | ||
essv7015018 | Submitted genomic | NC_000007.12:g.(?_ 125606775)_(125788 911_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 125,606,775 | 125,788,911 |