nsv3889814

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:170,444,751
  • Description:GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 AND not provided

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 421477 SVs from 147 studies. See in: genome view    
Remapped(Score: Good):165,632-170,610,382Question Mark
Overlapping variant regions from other studies: 420526 SVs from 147 studies. See in: genome view    
Submitted genomic165,632-170,919,470Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv3889814RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6165,632170,610,382
nsv3889814Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6165,632170,919,470

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15168255copy number gainMultipleMultiplenot providedPathogenicClinVarRCV000745404.13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15168255RemappedGoodNC_000006.12:g.(?_
165632)_(170610382
_?)dup
GRCh38.p12First PassNC_000006.12Chr6165,632170,610,382
nssv15168255Submitted genomicNC_000006.11:g.(?_
165632)_(170919470
_?)dup
GRCh37 (hg19)NC_000006.11Chr6165,632170,919,470

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15168255GRCh37: NC_000006.11:g.(?_165632)_(170919470_?)dupcopy number gainunknownnot providedPathogenicClinVarRCV000745404.13

No genotype data were submitted for this variant

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