esv3693275
- Organism: Homo sapiens
- Study:estd221 (Palta et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,788
- Publication(s):Palta et al. 2015
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: 510 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 510 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 186 SVs from 26 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 |
---|---|---|---|---|---|---|---|---|---|
esv3693275 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 52,828,661 | 52,848,448 |
esv3693275 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 53,331,914 | 53,351,701 |
esv3693275 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 58,023,726 | 58,043,513 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv16508132 | Remapped | Perfect | NC_000019.10:g.(?_ 52828661)_(5284844 8_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,828,661 | 52,848,448 |
essv16508132 | Remapped | Perfect | NC_000019.9:g.(?_5 3331914)_(53351701 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,331,914 | 53,351,701 |
essv16508132 | Submitted genomic | NC_000019.8:g.(?_5 8023726)_(58043513 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,023,726 | 58,043,513 |