esv2761965
- 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:15,114
- 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: 225 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 12 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 |
---|---|---|---|---|---|---|---|---|---|
esv2761965 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 162,310,935 | 162,326,048 |
esv2761965 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 162,280,725 | 162,295,838 |
esv2761965 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 160,547,349 | 160,562,462 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv7001699 | Remapped | Perfect | NC_000001.11:g.(?_ 162310935)_(162326 048_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 162,310,935 | 162,326,048 |
essv7001710 | Remapped | Perfect | NC_000001.11:g.(?_ 162314121)_(162326 048_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 162,314,121 | 162,326,048 |
essv7001699 | Remapped | Perfect | NC_000001.10:g.(?_ 162280725)_(162295 838_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 162,280,725 | 162,295,838 |
essv7001710 | Remapped | Perfect | NC_000001.10:g.(?_ 162283911)_(162295 838_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 162,283,911 | 162,295,838 |
essv7001699 | Submitted genomic | NC_000001.9:g.(?_1 60547349)_(1605624 62_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 160,547,349 | 160,562,462 | ||
essv7001710 | Submitted genomic | NC_000001.9:g.(?_1 60550535)_(1605624 62_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 160,550,535 | 160,562,462 |