nsv984844

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:133,742,557

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 243304 SVs from 114 studies. See in: genome view    
Remapped(Score: Good):26,823-133,769,379Question Mark
Overlapping variant regions from other studies: 240715 SVs from 114 studies. See in: genome view    
Remapped(Score: Good):72,759-135,506,704Question Mark
Overlapping variant regions from other studies: 108481 SVs from 44 studies. See in: genome view    
Submitted genomic62,759-135,356,694Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv984844RemappedGoodGRCh38 (hg38)Primary AssemblyFirst PassNC_000010.11Chr1026,823133,769,379
nsv984844RemappedGoodGRCh37 (hg19)Primary AssemblyFirst PassNC_000010.10Chr1072,759135,506,704
nsv984844Submitted genomicNCBI36 (hg18)NC_000010.9Chr1062,759135,356,694

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical
nssv459317copy number gainSNP arraySNP genotyping analysisLeukemia, Myeloid, Acutenot provided
nssv459362copy number gainSNP arraySNP genotyping analysisLeukemia, Myeloid, Acutenot provided

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv459317RemappedGoodNC_000010.11:g.(?_
26823)_(133769379_
?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000010.11Chr1026,823133,769,379
nssv459362RemappedGoodNC_000010.11:g.(?_
26823)_(133769379_
?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000010.11Chr1026,823133,769,379
nssv459317RemappedGoodNC_000010.10:g.(?_
72759)_(135506704_
?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000010.10Chr1072,759135,506,704
nssv459362RemappedGoodNC_000010.10:g.(?_
72759)_(135506704_
?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000010.10Chr1072,759135,506,704
nssv459317Submitted genomicNC_000010.9:g.(?_6
2759)_(135356694_?
)dup
NCBI36 (hg18)NC_000010.9Chr1062,759135,356,694
nssv459362Submitted genomicNC_000010.9:g.(?_6
2759)_(135356694_?
)dup
NCBI36 (hg18)NC_000010.9Chr1062,759135,356,694

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical Interpretation
nssv459317NC_000010.9:g.(?_62759)_(135356694_?)dupcopy number gainSomaticLeukemia, Myeloid, Acutenot provided
nssv459362NC_000010.9:g.(?_62759)_(135356694_?)dupcopy number gainSomaticLeukemia, Myeloid, Acutenot provided

No genotype data were submitted for this variant

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