esv2763265
- 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:170,605
- 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: 520 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 520 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 169 SVs from 18 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 |
---|---|---|---|---|---|---|---|---|---|
esv2763265 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 52,186,348 | 52,356,952 |
esv2763265 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 52,413,486 | 52,584,090 |
esv2763265 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 52,266,990 | 52,437,594 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv7013301 | Remapped | Perfect | NC_000002.12:g.(?_ 52186348)_(5235695 2_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 52,186,348 | 52,356,952 |
essv7013312 | Remapped | Perfect | NC_000002.12:g.(?_ 52221523)_(5227541 5_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 52,221,523 | 52,275,415 |
essv7013301 | Remapped | Perfect | NC_000002.11:g.(?_ 52413486)_(5258409 0_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 52,413,486 | 52,584,090 |
essv7013312 | Remapped | Perfect | NC_000002.11:g.(?_ 52448661)_(5250255 3_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 52,448,661 | 52,502,553 |
essv7013301 | Submitted genomic | NC_000002.10:g.(?_ 52266990)_(5243759 4_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 52,266,990 | 52,437,594 | ||
essv7013312 | Submitted genomic | NC_000002.10:g.(?_ 52302165)_(5235605 7_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 52,302,165 | 52,356,057 |