nsv4457273

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:137,922,076
  • Description:GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 AND not provided

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 297763 SVs from 144 studies. See in: genome view    
Remapped(Score: Good):203,861-138,125,936Question Mark
Overlapping variant regions from other studies: 298285 SVs from 144 studies. See in: genome view    
Submitted genomic203,861-141,020,388Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4457273RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9203,861138,125,936
nsv4457273Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9203,861141,020,388

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15777263copy number gainMultipleMultiplenot providedPathogenicClinVarRCV000845900.13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15777263RemappedGoodNC_000009.12:g.(?_
203861)_(138125936
_?)dup
GRCh38.p12First PassNC_000009.12Chr9203,861138,125,936
nssv15777263Submitted genomicNC_000009.11:g.(?_
203861)_(141020388
_?)dup
GRCh37 (hg19)NC_000009.11Chr9203,861141,020,388

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15777263GRCh37: NC_000009.11:g.(?_203861)_(141020388_?)dupcopy number gainunknownnot providedPathogenicClinVarRCV000845900.13

No genotype data were submitted for this variant

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