nsv959642
- 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:328,466
- 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: 903 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 903 SVs from 62 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 |
---|---|---|---|---|---|---|---|---|---|
nsv959642 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 88,612,717 | 88,941,182 |
nsv959642 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 89,322,436 | 89,650,901 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv3021518 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv3021518 | Remapped | Perfect | NC_000006.12:g.(88 145276_88612717)_( 88941182_88963344) dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 88,145,276 | 88,612,717 | 88,941,182 | 88,963,344 |
nssv3021518 | Submitted genomic | NC_000006.11:g.(88 854995_89322436)_( 89650901_89673063) dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 88,854,995 | 89,322,436 | 89,650,901 | 89,673,063 |