esv34506
- Organism: Homo sapiens
- Study:estd55 (Pinto et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:277,851
- Description:Sample level SV from stringent call set
- Publication(s):Pinto 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: 1205 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 1205 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 55 SVs from 8 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 |
---|---|---|---|---|---|---|---|---|---|
esv34506 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 57,160,644 | 57,438,494 |
esv34506 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 57,387,779 | 57,665,629 |
esv34506 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000002.9 | Chr2 | 57,299,430 | 57,577,280 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv6978714 | Remapped | Perfect | NC_000002.12:g.(?_ 57160644)_(5743849 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 57,160,644 | 57,438,494 |
essv6978715 | Remapped | Perfect | NC_000002.12:g.(?_ 57175190)_(5721450 8_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 57,175,190 | 57,214,508 |
essv6990275 | Remapped | Perfect | NC_000002.12:g.(?_ 57175214)_(5721451 4_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 57,175,214 | 57,214,514 |
essv6978714 | Remapped | Perfect | NC_000002.11:g.(?_ 57387779)_(5766562 9_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 57,387,779 | 57,665,629 |
essv6978715 | Remapped | Perfect | NC_000002.11:g.(?_ 57402325)_(5744164 3_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 57,402,325 | 57,441,643 |
essv6990275 | Remapped | Perfect | NC_000002.11:g.(?_ 57402349)_(5744164 9_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 57,402,349 | 57,441,649 |
essv6978714 | Submitted genomic | NC_000002.9:g.(?_5 7299430)_(57577280 _?)dup | NCBI35 (hg17) | NC_000002.9 | Chr2 | 57,299,430 | 57,577,280 | ||
essv6978715 | Submitted genomic | NC_000002.9:g.(?_5 7313976)_(57353294 _?)dup | NCBI35 (hg17) | NC_000002.9 | Chr2 | 57,313,976 | 57,353,294 | ||
essv6990275 | Submitted genomic | NC_000002.9:g.(?_5 7314000)_(57353300 _?)dup | NCBI35 (hg17) | NC_000002.9 | Chr2 | 57,314,000 | 57,353,300 |