nsv959876
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:367,036
- Publication(s):Poultney et al. 2013
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: 927 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 930 SVs from 68 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 |
---|---|---|---|---|---|---|---|---|---|
nsv959876 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 61,680,961 | 62,047,996 |
nsv959876 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 62,390,866 | 62,757,901 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv3021307 | duplication | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv3021307 | Remapped | Pass | NC_000006.12:g.(57 788605_60531288)_( 62177183_62177183) dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 57,788,605 | 60,531,288 | 62,177,183 | 62,177,183 |
nssv3021307 | Submitted genomic | NC_000006.11:g.(57 499035_62390866)_( 62757901_62887088) dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 57,499,035 | 62,390,866 | 62,757,901 | 62,887,088 |