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nsv3889911

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:540
  • Description:GRCh37/hg19 6p25.3(chr6:2207469-2208008)x0 AND not provided

Genome View

Select assembly:
Overlapping variant regions from other studies: 141 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):2,207,235-2,207,774Question Mark
Overlapping variant regions from other studies: 141 SVs from 31 studies. See in: genome view    
Submitted genomic2,207,469-2,208,008Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv3889911RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr62,207,2352,207,774
nsv3889911Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr62,207,4692,208,008

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15166703copy number lossMultipleMultiplenot providedBenignClinVarRCV000745423.2, VCV000608787.20

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15166703RemappedPerfectNC_000006.12:g.(?_
2207235)_(2207774_
?)del
GRCh38.p12First PassNC_000006.12Chr62,207,2352,207,774
nssv15166703Submitted genomicNC_000006.11:g.(?_
2207469)_(2208008_
?)del
GRCh37 (hg19)NC_000006.11Chr62,207,4692,208,008

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15166703GRCh37: NC_000006.11:g.(?_2207469)_(2208008_?)delcopy number lossunknownnot providedBenignClinVarRCV000745423.2, VCV000608787.20

No genotype data were submitted for this variant

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