nsv4603739
- Organism: Homo sapiens
- Study:nstd183 (DECIPHER Consensus CNVs)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:153,936
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: 474 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 474 SVs from 60 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4603739 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 5,984,675 | 6,138,610 |
| nsv4603739 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 6,005,905 | 6,159,840 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16115504 | deletion | Curated | Curated |
| nssv16117554 | duplication | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16115504 | Remapped | Perfect | NC_000011.10:g.(?_ 5984675)_(6138610_ ?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 5,984,675 | 6,138,610 |
| nssv16117554 | Remapped | Perfect | NC_000011.10:g.(?_ 5984675)_(6138610_ ?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 5,984,675 | 6,138,610 |
| nssv16115504 | Submitted genomic | NC_000011.9:g.(?_6 005905)_(6159840_? )del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 6,005,905 | 6,159,840 | ||
| nssv16117554 | Submitted genomic | NC_000011.9:g.(?_6 005905)_(6159840_? )dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 6,005,905 | 6,159,840 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16115504 | <0.001 | 1 | 5919 |
| nssv16117554 | <0.001 | 2 | 5919 |