nsv3137767
- Organism: Homo sapiens
- Study:nstd151 (Exome Aggregation Consortium CNVs)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,420
- Description:qual score = 88
- Publication(s):Exome Aggregation Consortium CNVs
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: 142 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 142 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3137767 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 43,970,593 | 43,978,012 |
| nsv3137767 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 44,436,265 | 44,443,684 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv14128180 | copy number gain | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14128180 | Remapped | Perfect | NC_000001.11:g.(?_ 43970593)_(4397801 2_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 43,970,593 | 43,978,012 |
| nssv14128180 | Submitted genomic | NC_000001.10:g.(?_ 44436265)_(4444368 4_?)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 44,436,265 | 44,443,684 |