esv2755386
- Organism: Homo sapiens
- Study:estd55 (Pinto et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:395,001
- 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: 1158 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 1158 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 43 SVs from 6 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2755386 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 145,606,259 | 146,001,259 |
| esv2755386 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 145,303,352 | 145,698,352 |
| esv2755386 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000007.11 | Chr7 | 144,741,000 | 145,136,000 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv6986826 | Remapped | Perfect | NC_000007.14:g.(?_ 145606259)_(146001 259_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 145,606,259 | 146,001,259 |
| essv6986826 | Remapped | Perfect | NC_000007.13:g.(?_ 145303352)_(145698 352_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 145,303,352 | 145,698,352 |
| essv6986826 | Submitted genomic | NC_000007.11:g.(?_ 144741000)_(145136 000_?)dup | NCBI35 (hg17) | NC_000007.11 | Chr7 | 144,741,000 | 145,136,000 |