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nsv4728205

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:354,240
  • Description:GRCh37/hg19 3q23-24(chr3:142542265-142896504)x3 AND not provided

Genome View

Select assembly:
Overlapping variant regions from other studies: 954 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):142,823,423-143,177,662Question Mark
Overlapping variant regions from other studies: 954 SVs from 80 studies. See in: genome view    
Submitted genomic142,542,265-142,896,504Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4728205RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3142,823,423143,177,662
nsv4728205Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3142,542,265142,896,504

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv16255261copy number gainMultipleMultiplenot providedUncertain significanceClinVarRCV001259241.1, VCV000980065.13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv16255261RemappedPerfectNC_000003.12:g.(?_
142823423)_(143177
662_?)dup
GRCh38.p12First PassNC_000003.12Chr3142,823,423143,177,662
nssv16255261Submitted genomicNC_000003.11:g.(?_
142542265)_(142896
504_?)dup
GRCh37 (hg19)NC_000003.11Chr3142,542,265142,896,504

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv16255261GRCh37: NC_000003.11:g.(?_142542265)_(142896504_?)dupcopy number gaingermlinenot providedUncertain significanceClinVarRCV001259241.1, VCV000980065.13

No genotype data were submitted for this variant

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