esv29963
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:16,090
- Publication(s):Levy et al. 2007
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: 595 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 324 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 595 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 374 SVs from 20 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 |
---|---|---|---|---|---|---|---|---|---|
esv29963 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 143,538,013 | 143,554,102 |
esv29963 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187571.1 | Chr8|NT_18 7571.1 | 28,053 | 44,142 |
esv29963 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 144,620,183 | 144,636,272 |
esv29963 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 144,691,326 | 144,707,415 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv84202 | Remapped | Perfect | NT_187571.1:g.(?_2 8053)_(44142_?)del | GRCh38.p12 | Second Pass | NT_187571.1 | Chr8|NT_18 7571.1 | 28,053 | 44,142 |
essv84202 | Remapped | Perfect | NC_000008.11:g.(?_ 143538013)_(143554 102_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 143,538,013 | 143,554,102 |
essv84202 | Remapped | Perfect | NC_000008.10:g.(?_ 144620183)_(144636 272_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 144,620,183 | 144,636,272 |
essv84202 | Submitted genomic | NC_000008.9:g.(?_1 44691326)_(1447074 15_?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 144,691,326 | 144,707,415 |