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nsv233

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,064

Genome View

Select assembly:
Overlapping variant regions from other studies: 173 SVs from 39 studies. See in: genome view    
Remapped(Score: Good):50,857,780-50,888,843Question Mark
Overlapping variant regions from other studies: 163 SVs from 35 studies. See in: genome view    
Remapped(Score: Pass):50,895,211-50,924,187Question Mark
Overlapping variant regions from other studies: 3 SVs from 3 studies. See in: genome view    
Submitted genomic50,870,215-50,901,282Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StopOuter Stop
nsv233RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr350,857,780-50,888,843
nsv233RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr350,895,21150,924,187-
nsv233Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000003.9Chr350,870,215-50,901,282

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv233inversionSAMN00000376SequencingPaired-end mapping297

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StopOuter Stop
nssv233RemappedGoodNC_000003.12:g.(50
857780_?)_(?_50888
843)inv
GRCh38.p12First PassNC_000003.12Chr350,857,780-50,888,843
nssv233RemappedPassNC_000003.11:g.(50
895211_?)_(5092418
7_?)inv
GRCh37.p13First PassNC_000003.11Chr350,895,21150,924,187-
nssv233Submitted genomicNC_000003.9:g.(508
70215_?)_(?_509012
82)inv
NCBI35 (hg17)NC_000003.9Chr350,870,215-50,901,282

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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