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nsv3891842

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:138,206,633
  • Description:GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 AND not provided

Genome View

Select assembly:
Overlapping variant regions from other studies: 327194 SVs from 149 studies. See in: genome view    
Remapped(Score: Good):10,590-138,217,222Question Mark
Overlapping variant regions from other studies: 327190 SVs from 149 studies. See in: genome view    
Submitted genomic10,590-141,107,672Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv3891842RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr910,590138,217,222
nsv3891842Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr910,590141,107,672

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15169725copy number gainMultipleMultiplenot providedPathogenicClinVarRCV000748053.2, VCV000611417.23

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15169725RemappedGoodNC_000009.12:g.(?_
10590)_(138217222_
?)dup
GRCh38.p12First PassNC_000009.12Chr910,590138,217,222
nssv15169725Submitted genomicNC_000009.11:g.(?_
10590)_(141107672_
?)dup
GRCh37 (hg19)NC_000009.11Chr910,590141,107,672

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15169725GRCh37: NC_000009.11:g.(?_10590)_(141107672_?)dupcopy number gainunknownnot providedPathogenicClinVarRCV000748053.2, VCV000611417.23

No genotype data were submitted for this variant

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