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nsv6315535

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:26,628,985
  • Description:GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 80542 SVs from 146 studies. See in: genome view    
Remapped(Score: Good):230,615-26,859,599Question Mark
Overlapping variant regions from other studies: 80197 SVs from 146 studies. See in: genome view    
Submitted genomic230,615-26,881,146Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv6315535RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11230,61526,859,599
nsv6315535Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr11230,61526,881,146

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv17976735copy number gainMultipleMultipleSee casesPathogenicClinVarRCV002286351.1, VCV001707435.13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv17976735RemappedGoodNC_000011.10:g.(23
0615_?)_(?_2685959
9)dup
GRCh38.p12First PassNC_000011.10Chr11230,61526,859,599
nssv17976735Submitted genomicNC_000011.9:g.(230
615_?)_(?_26881146
)dup
GRCh37 (hg19)NC_000011.9Chr11230,61526,881,146

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv17976735GRCh37: NC_000011.9:g.(230615_?)_(?_26881146)dupcopy number gainunknownSee casesPathogenicClinVarRCV002286351.1, VCV001707435.13

No genotype data were submitted for this variant

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